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Artículos
Schoolcraft WB, Fragouli E, Stevens J, Munné S, Katz-Jaffe MG, Wells D (2010) Clinical application of comprehensive chromosomal screening at the blastocyst stage. Fertil steril, In press
Magli MC, Gianaroli L, Crippa A, Munné S, Robles F, Ferraretti AP (2010) Aneuploidies of chromosomes 1, 4 and 6 are not compatible with human embryos’ implantation. Fertil Steril In press
Fragouli E, Alfarawati S, Katz-Jaffe M, Stevens J, Colls P, Goodall N, Tormasi S, Gutierrez-Mateo C, Prates R, Schoolcraft WB, Munné M, Wells D (2010) Comprehensive chromosome screening of polar bodies and blastocysts from couples experiencing repeated implantation failure. Fertil Steril In press
Munné S, Fragouli E, Colls P, Katz M, Schoocraft W, Wells D (2010) Comprehensive chromosome screening indicates that an appropriately designed 12-chromosome FISH test would detect 91% of aneuploid blastocysts. Reprod Biomed Online In press
Fischer J, Colls P, Escudero T, Munné S (2010) Preimplantation Genetic Diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses. Fertil Steril, In press
Munné S, Wells D, Cohen J (2010) Technology requirements for preimplantation genetic diagnosis to improve art outcome. Fertil steril, In press
Lu CM, Kwan J, Baumgartner A, Weier JF, Wang M, Escudero T, Munné S, Zitzelsberger HF, and Weier HUG (2010) DNA Probe Pooling for Rapid Delineation of Chromosomal Breakpoints. JHC, In press
McWeeney DT, Munné S, Miller R, Cekleniak NA, Contag SA, Wax JR, Polzin WJ, Watson WJ (2010) Pregnancy Complicated by Triploidy: A Comparison of the Three Karyotypes. Am J Perinatology In press
Colls P, Silver L, Olivera G, Weier J, Escudero T, Goodall N, Tomkin G, Munné S (2009) Preimplantation genetic diagnosis of gender selection in the united states. Reprod Biomed Online 19:16-22
McWeeney DT, Munné S, Miller R, Cekleniak NA, Contag SA, Wax JR, Polzin WJ, Watson WJ (2009) Pregnancy Complicated by Triploidy: A Comparison of the Three Karyotypes. Am J Perinatology 9:641-645
Gutierrez C; Sánchez-García J; Fischer J; Tormasi S; Cohen J, Ph.D.; Munné S; Wells D (2009) Preimplantation genetic diagnosis (PGD) of single gene disorders: experience with over 200 cycles conducted by a reference laboratory in the United States. Fertil Steril 92:1544–56
Colls P, Goodall N, Zheng X, Munné S (2009) Increased efficiency of preimplantation genetic diagnosis for aneuploidy by testing 12 chromosomes. Reprod Biomed Online 19:532-538
Weghofer A, Munné S, Brannath W, Chen S, Barad D, Cohen J, Gleicher N (2009) The impact of LH-containing gonadotropin stimulation on euploidy rates in preimplantation embryos: antagonist cycles. Ferti Steril 92:937-942
Garrisi GJ, Colls P, Ferry KM, Zheng X, Garrisi MG, Munné S (2009) Effect of infertility, maternal age and number of previous miscarriages on the outcome of preimplantation genetic diagnosis for idiopathic recurrent pregnancy loss. Fertil Steril 92:288-295
Schoolcraft WB, Katz-Jaffe MG, Stevens J, Rawlins M, Munné S (2009) Preimplantation genetic diagnosis for aneuploidy screening: a randomized prospective trial. Fertil Steril 92:157-162
Munné S, Tomkin G, Cohen J (2009) Selection Of Embryos By Morphology Is Less Effective Compared To A Combination Of Aneuploidy Testing And Morphology Observations. Fertil Steril 91:943-945
Fragouli E, Escalona A, Gutierrez-Mateo C, Tormasi S, Alfarawati S, Sepulveda S, Noriega L4, Garcia J, Wells D, Munné S (2009) Comparative genomic hybridization of oocytes and first polar bodies from young donors. Reprod Biomed Online, 18: 228-237
Munné S (2009) Preimplantation genetic diagnosis for infertility (PGS). In: Current Status of Preimplantation Genetic Diagnosis (PGD) Harper J (Ed). Cambridge University Press. Chapter 13, pp: 203-229
Munné S, Howles CM, Wells D (2009) The role of preimplantation genetic diagnosis in diagnosing embryo aneuploidy. Cur Op Ob Gyn 21:442-449
Ferraretti AP, Gianaroli L, Magli C, Farfalli V, Lappi M, Munne S (2008) PGD for chromosome anomalies. In: Infertility and Assisted Reproduction. Edited by: Rizk B, Garcia-Velasco J, Sallam H, Makrigiannakis A. chapter 65, pp. 643-656
Lopez P, Munne S (2008) Eficiencia del diagnostico preimplantacional (DGP) en infertilidad. In: Fertilidad y Reproducción asistida. Lerner J, Urbina MT Eds. Sociedad de Obstetricia Y Ginecologia de Venezuela. Editorial Medica Panamericana, Venezuela. Pp 573-575
Garrisi GJ, Colls P, Ferry KM, Zheng X, Garrisi MG, Munné S (2008) Effect of infertility, maternal age and number of previous miscarriages on the outcome of preimplantation genetic diagnosis for idiopathic recurrent pregnancy loss. Fertil Steril In press (74)
The Preimplantation Genetic Diagnosis International Society (PGDIS*) (2008) Guidelines for good practice in PGD: program requirements and laboratory quality assurance. Reproductive Biomed Online 16:134-147 (73) (*Drs. Munne are officers in that society and prepared this document)
Escudero T, Estop A, Fischer J, Munne S (2008) Preimplantation Genetic Diagnosis for complex chromosome rearrangements. Am J Medical Genetics 146a:1662-1669
Cohen J, Grifo J (2007) Multicnetre trial of preimplantation genetic screening reported in the New England Journal of Medicine: an in depth look at the findings. Reproductive Biomed Online 15:365-366
Munné S, Gianaroli L, Tur-Kaspa I, Magli C, Sandalinas M, Grifo J, Cram D, Kahraman S, Verlinsky Y, Simpson JL (2007) Sub-standard application of PGS may interfere with its clinical success. Fertil Steril 88:781-784
Cohen J, Wells D, Munné S (2007) Removal of two cells from cleavage stage embryos is likely to reduce the efficacy of chromosomal tests employed to enhance implantation rates. Fertil Steril, 87:496-503
Munné S, Serena C, Colls P, Garrisi J, Zheng X, Cekleniak N, Lenzi M, Hughes P2, Fischer J, Garrisi M, Tomkin G, Cohen J (2007) Maternal age, morphology, development and chromosome abnormalities in over 6000 cleavage-stage embryos. Reproductive Biomedicine Online 14:628-634
Munné S, Ary J, Zouves C, Escudero T, Barnes F, Cinioglu C, Ary B, Cohen J (2006) Wide range of chromosome abnormalities in the embryos of young egg donors. Reproductive Biomed Online, 12:340-346
Munné S (2006) Chromosome abnormalities and their relationship to morphology and development of human embryos. Reproductive Biomedicine Online 12:234-253
Munné S, Fischer J, Warner A, Chen S, Zouves C, Cohen J, And referring centers PGD group (2006) Preimplantation Genetic Diagnosis Significantly Reduces Pregnancy Loss in Infertile Couples: A Multi-Center Study. Fertil Steril 85:326-332
Munne, S. (2005) Preimplantation genetic diagnosis for chromosome abnormalities. In Jorde, L.B., Little, P.F.R., Dunn, M.J. and Subramaniam, S. (Eds), Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics. John Wiley & Sons Ltd: Chichester, volume , pp. 176. (60b)
Munné S (2005) Analysis of the segregation of chromosomes during preimplantation genetic diagnosis in both male and female translocation heterozygotes. Cytogenetics and Genomic Res 305-309
Stachecki J, Cohen J, Munne S (2005) Cryopreservation of biopsied cleavage stage biopsied embryos. Reproductive Biomed online 6:711-715
Chen SH, Escudero T, Cekleniak NA, Sable DB, Garrisi MG, Cohen J, Munné S (2005) Maternal balanced translocation is a risk factor for poor response to ovarian stimulation. Fertil Steril 83:1504-1509
Munné S, Chen S, Fischer J, Colls P, Zheng X, Stevens J, Escudero T, Oter M, Schoolcraft W, Simpson JL, Cohen J (2005) Preimplantation genetic diagnosis reduces pregnancy loss in women 35 and older with a history of recurrent miscarriages. Fertil Steril 84:331-335
Gutiérrez-Mateo C, Gadea L, Benet J, Wells D, Munné S, Navarro J (2005) Aneuploidy 12 in a Robertsonian (13;14) carrier: Case Report. Human Reprod 20:1256-1260
Weier HUG, Weier JF, Oter Renom M, Zheng X, Colls P, Nureddin A, Pham CD, Chu LW, Racowsky C, Munné S (2005) Fluorescence in situ hybridization and spectral imaging analysis of human oocytes and first polar bodies. J Histochem Cytochem 53:269-272
Munné S, Escudero T, Fischer J, Chen S, Hill J, Stelling JR, Estop E (2005) Negligible interchromosomal effect in embryos of Robertsonian translocation carriers. Reprod Biomed Online 10:363-369
Munné S, Cohen J (2004) The status of Preimplantation Genetic Diagnosis in Japan: a criticism. Reprod Biomed Online 9:258-259
Stachecki J, Munné S, Cohen J (2004) Spindle organization after cryopreservation of mouse, human, and bovine oocytes. Reprod Biomed Online 8:664-672
Gutiérrez CM, Wells D, Benet J, Sánchez-García JF, Bermúdez MG, Belil I, Egozcue J, Munné S, Navarro J (2004) Reliability of Comparative Genomic Hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes. Human Reprod 19:2118-2125
Gutiérrez-Mateo C, Benet J, Wells D, Colls P, Bermúdez MG, Sánchez-García JF, Egozcue J, Navarro J, Munné S (2004) Aneuploidy study of human oocytes first polar body comparative genomic hybridization and metaphase II fluorescence in situ hybridization analysis. Human Reprod 19:2859-2868
Munné S, Sandalinas M, Magli M, Gianaroli L, Cohen J, Warburton D (2004) Increased rate of aneuploid embryos in young women with previous aneuploid conceptions. Prenat Diagn. 24:638-647
Weier HUG, Weier JF, Oter Renom M, Zheng X, Colls P, Nureddin A, Pham CD, Chu LW, Racowsky C, Munné S (2004) Fluorescence in situ hybridization and spectral image analysis of human oocytes and first polar bodies. J Histochem Cytochem 52:1-4
Colls P, Sandalinas M, Pagidas K, Munné S (2004) PGD analysis for aneuploidy in a patient heterozygous for a polymorphism of chromosome 16 (16qh-). Prenat Diagn 24:741-744
Bermúdez MG, Wells D, Malter H, Munné S, Cohen J, Steuerwald NM (2004) Expression Profiles of Individual Human Oocytes using Microarray Technology. Reproductive Biomedicine Online. Online 8:325-337
Santiago Munné, Muhterem Bahçe, Mireia Sandalinas, Tomás Escudero, Carmen Márquez, Esther Velilla, Pere Colls, Maria Oter, Mina Alikani, Jacques Cohen (2004) Differences in chromosome susceptibility to aneuploidy and survival to first trimester. Reproductive Biomedicine Online, 8:81-90
Werlin L, Rodi I, DeCherney A, Marello E, Hill D, Munné S (2003) Preimplantation genetic diagnosis (PGD) as both a therapeutic and diagnostic tool in assisted reproductive technology. Fertil Steril, 80 :467-468
Munné S, Sandalinas M, Escudero T, Velilla E, Walmsley R, Sadowy S, Cohen J, Sable D (2003) Improved implantation after preimplantation genetic diagnosis of aneuploidy. Reprod Biomed Online, 7:91-97
Escudero T, Abdelhadi I, Sandalinas M, Munné S (2003) Predictive value of sperm chromosome analysis on the outcome of PGD for translocations. Fertil Steril 79:1528-1534
AbdelhadiI I, Colls P, Sandalinas M, Escudero T, Munné S. Preimplantation genetic diagnosis of numerical abnormalities for 13 chromosomes. Reprod Biomed online, 2003: 6:226-231
Silber S, Escudero T, Lenahan K, Sadowy S, Abdelhadi I, Kilani Z, Munné S (2003) Chromosomal abnormalities in embryos derived from TESE. Fertil Steril, 30-38
Wells D, Escudero T, Levy B, Hirschhorn K, Delhanty JDA, Munné S (2002) First clinical application of comparative genome hybridization (CGH) and polar body testing for Preimplantation genetic diagnosis (PGD) of aneuploidy. Fertil Steril 78, 543-549
Munné S, Cohen J, Sable D (2002) Preimplantation Genetic Diagnosis for advanced maternal age and other indications. Fertil Steril 78:234-236
Munné S, Wells D (2002) Preimplantation genetic diagnosis. Current Opinion Obstet Gynecol 14: 239-244
Velilla E, Escudero T, Munné S (2002)Blastomere fixation techniques and risk of misdiagnosis for PGD of Aneuploidy. Reprod Biomed Online, 4:210-217
Munné S, Sandalinas M, Escudero T, Marquez C, Cohen J (2002)Chromosome mosaicism in cleavage stage human embryos: evidence of a maternal age effect. Reprod Biomed Online 4:223-232
Sandalinas M, Márquez M, Munné S (2002) Spectral karyotyping of unfertilized and non-inseminated oocytes. Molec Human Reprod, 8:580-585
Munné S (2002) Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities. Reprod Biomed Online 4:183-196
Magli MC, Sandalinas M, Escudero T, Morrison L, Ferraretti AP, Gianaroli L, Munné S (2001) Double locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy. Prenatal diagnosis 21:1080-1085
Munné S (2001) Preimplantation genetic diagnosis of Structural abnormalities. Molec Cell endocrinol 183: S55-S58
Weier HUG, Munné S, Lersch RA, Hsieh HB, Smida J, Chen XN, Korenberg JR, Pedersen RA, Fung J (2001) Towards a full karyotype screening of interphase cells: 'FISH and chip' technology. Molec Cell Endocrinol. 183: S41-S45
Escudero T, Lee M, Stevens J, Sandalinas M, Munné S (2001) Preimplantation Genetic diagnosis of pericentric inversions. Prenatal Diagnosis 21:760-766
Sandalinas M, Sadowy S, Alikani M, Calderon G, Cohen J, Munné S. (2001) Developmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage. Human Reprod, 16:1954-1958
Obasaju M, Kadam A, Biancardi T, Sultan K, Fateh M, Munné S (2001) Pregnancy rate from the transfer of a single normal embryo in women over 40 years of age undergoing PGD for chromosomal abnormalities. Reproductive Biomedicine Online 2:98-101
Munné S, Escudero T, Sandalinas M, Sable D, Cohen J (2000) Gamete segregation in female carriers of Robertsonian translocations. Cytogenet Cell Genet 90:303-308
Márquez C, Sandalinas M, Bahçe M, Alikani M, Munné S (2000) Chromosome abnormalities in 1255 cleavage-stage human embryos. Reproductive Biomedicine Online 1:17-27
Bahçe M, Escudero T, Sandalinas M, Morrison L, Legator M, Munné S (2000) Improvements of preimplantation diagnosis of aneuploidy by using microwave-hybridization, cell recycling and monocolor labeling of probes. Molec Human Reprod 9:849-854
Munné S, Sepulveda S, Balmaceda J, Fernandez E, Fabres C, Mackenna A, Lopez T, Crosby JA, Zegers-Hochschild F (2000) Selection of the most common chromosome abnormalities in oocytes prior to ICSI. Prerat Diagn 20:582-586
Escudero T, Lee L, Carrel D, Blanco J, Munné S (2000) Analysis Of Chromosome Abnormalities In Sperm And Embryos From Two 45,XY,t(13;14)(q10;q10) Carriers. Prenat Diagn 20:599-602
Munné S, Sandalinas M, Escudero T, Fung J, Gianaroli L, Cohen J (2000) Outcome of preimplantation genetic diagnosis of translocations. Fertil Steril. 73:1209-1218
Lee M, Munné S (2000) Pregnancy after polar body biopsy and freezing and thawing of human embryos. Fertil Steril 73:645-647
Escudero T, Lee Michael L, Sandalinas S, Munné S (2000) Female gamete segregation in two carriers of translocations involving 2q and 14q. Prenat Diagn, 20:235-237
Obasaju M, Kadam A, Sultan K, Fateh M, Munné S (1999) Evidence that sperm quality may adversely affect the chromosome constitution of embryos resulting from ICSI. Fertil. Steril. 1113-1115
Gianaroli L, Magli MC, Ferraretti AP, Munné S (1999) Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with poor prognosis: identification of the categories to which it should be proposed. Fertil. Steril. 72:837-844
Munné S, Magli C, Cohen J, Morton P, Sadowy S, Gianaroli L, Tucker M, Márquez C, Sable D, Ferraretti AP, Massey JB, Scott R (1999) Positive outcome after preimplantation diagnosis of aneuploidy in human embryos. Human Reprod, 14:2191-2199
Gianaroli L, Magli MC, Munné S, Fortini D, Ferraretti AP (1999) Advantages of day four embryo transfer in patients undergoing preimplantation genetic diagnosis of aneuploidy. J. Assisted Reprod Genet 16:170-175
Weier HUG, Munné S, Fung J (1999) patient-specific probes for Preimplantion genetic diagnosis (PGD) of structural and numerical aberrations in interphase cells. J. Assisted Reprod Genet 16:182-191
Bahçe M, Cohen J, Munné S (1999) PGD of aneuploidy: were we looking at the wrong chromosomes? J. Assisted Reprod Genet. 16: 176-181
Magli MC, Gianaroli L, Ferraretti AP, Fortini D, Munné S (1999) Impact of blastomere biopsy and cryopreservation techniques on human embryo viability. Human Reprod. 14:770-773
Willadsen S, Levron J, Munné S, Schimmel T, Márquez C, Scott R, Cohen J (1999) Rapid Visualization of Metaphase Chromosomes in Single Human Blastomeres After Fusion with In Vitro Matured Bovine Eggs. Human Reprod 14:470-475
Munné S and Cohen J (1998) Chromosome abnormalities in human embryos. Human Reprod Update. 4: 842-855
Munné S, Magli C, Bahçe M, Fung J, Legator M, Morrison L, Cohen J, Gianaroli L (1998) Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13, 14, 15, 16, 18, 21, 22. Prenat Diagn. 18:1459-1466
Cohen J, Scott R, Alikani M. Schimmel T, Munné S, Levron J, Wu L, Brenner C, Warner C, Willadsen S (1998) Ooplasmic transfer in mature human oocytes. Molec Human Reprod 4: 269-280
Munné S, Márquez C, Magli C, Morton P, Morrison (1998) Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X, Y, 13, 16, 18 and 21. Human Molec Reprod 9:863-870
Márquez C, Cohen J, Munné S (1998) Chromosome identification on human oocytes and polar bodies by spectral karyotyping. Cytogenet Cell Genet 81:254-258
Munné S, Fung J, Cassel MJ, Márquez C, Weier HUG (1998) Preimplantation Genetic Analysis of Translocations: Case-Specific Probes for Interphase Cell Analysis. Human Genet, 102:663-674
Magli MC, Gianaroli L, Munné S, Ferraretti AP (1998) Incidence of chromosomal abnormalities from a morphologically normal cohort of embryos in poor-prognosis patients. J Assist Reprod Genet 15:297-301
Munné S, Morrison L, Fung J, Márquez C, Weier U, Bahçe M, Sable D, Grundfelt L, Schoolcraft, Scott R, Cohen J (1998). Spontaneous abortions are reduced after pre-conception diagnosis of translocations. J Assist Reprod Genet 290-296
Munné S, Márquez C, Reing A, Garrisi J, Alikani M (1998) Chromosome abnormalities in embryos obtained following conventional IVF and ICSI. Fertil Steril 69:904-908
Estop AM, Munné S, Cieply KM, Vandermark KK, Lamb AN, Fisch H (1998) Meiotic products of Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis. Human Reprod. 13: 124-127
Munné S, Scott R, Sable D, Cohen J (1998) First pregnancies after pre-conception diagnosis of translocations of maternal origin. Fertil Steril 69:675-681
Gianaroli L, Munné S, Magli MC, Ferraretti AP (1997) Preimplantation genetic diagnosis of aneuploidy and male infertility. Int.J.Androl. 20:Suppl.3:31-34
Gianaroli L, Magli MC, Ferraretti AP, Fiorentino A, garrisi J, Munné S (1997) Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos. Fertil.Steril. 68:1128-1131
Cassel MJ, Munné S, Fung J, Weier HUG (1997) Carrier-specific breakpoint-spanning DNA probes: an approach to preimplantation genetic diagnosis in interphase cells. Human Reprod 2019-2027
Gianaroli L, Magli MC, Munné S, Fiorentino A, Montanaro N, Ferraretti AP (1997) Will preimplantation genetic diagnosis assist patients with a poor prognosis to achieve pregnancy? Hum Reprod 12:1762-1767
Munné S, Magli C, Adler A, Wright G, de Boer K, Mortimer D, Tucker M, Cohen J, Gianaroli L (1997) Treatment-related chromosome abnormalities in human embryos. Human Reprod, 12:780-784
Munné S, Weier, U (1996) Simultaneous enumeration of chromosomes 13, 18, 21, X and Y in interphase cells for preimplantation genetic diagnosis of aneuploidy. Cytogenet. Cell. Genet 75:263-270
Templado C, Marquez C, Munné S, Colls P, Martorell MR, Cieply K, Benet J, Van Kirk V, Navarro J, Estop AM (1996) An analysis of human sperm chromosome aneuploidy. Cytogenet Cell Genet 74:194-200
Dailey T, Dale B, Cohen J and Munné S (1996) Association between non-disjunction and maternal age in meiosis-II human oocytes detected by FISH analysis. Am.J.Hum.Genet, 59:176-184
Kligman I, Benadiva C, Alikani M, Munné S (1996) The presence of multinucleated blastomeres in human embryos correlates with chromosomal abnormalities. Human Reprod, 11:1492-1498.
Benadiva C, Kligman I, Grifo J, Munné S (1996) Aneuploidy 16 in human embryos increases significantly with maternal age. Fertil. Steril. 66:248-255
Munné S, Dailey T, Finkelstein M, Weier HUG (1996) Reduction in signal overlap results in increased FISH efficiency: implications for preimplantation genetic diagnosis. J. Assisted Reprod. Genet. 13:149-156.
Munné S, Alonso ML, Grifo J (1996) case report: unusually high rates of aneuploid embryos in a 28-year old woman with incontinentia pigmenti. Cytogenet. Cell Genet., 72:43-45
Munné S, Alikani M, Tomkin G, Grifo J, Cohen J (1995) Embryo morphology, developmental rates and maternal age are correlated with chromosome abnormalities. Fertil.Steril., 64:382-391
Munné S, Dailey T, Sultan KM, Grifo J, Cohen J.(1995) The use of first polar bodies for preimplantation diagnosis of aneuploidy. Human Reprod. 10:1015-1021
Munné S, Sultan KM, Weier HUG, Grifo J, Cohen J, Rosenwaks Z (1995) Assessment of numerical abnormalities of X, Y, 18 and 16-chromosomes in preimplantation human embryos prior transfer. Am. J. Obs. Gyn 172:1191-1201
Grifo JA, Tang YX, Munné S, Alikani M, Cohen J , Rosenwaks Z (1994) Healthy deliveries from biopsied human embryos. Hum.Reprod. 9:912-916
Palermo G, Munné S and Cohen J (1994) The human zygote inherits its mitotic potential from the male gamete. Hum.Reprod. 9:1220-1225.
Munné S, Weier HUG, Grifo J, Cohen J (1994) Chromosome mosaicism in human embryos. Biol. Reprod. 51:373-379
Munné S, Grifo J, Cohen J, Weier HUG (1994) Chromosome abnormalities in Arrested Human Preimplantation Embryos: A Multiple Probe Fluorescence In Situ Hybridization (FISH) Study. Am.J.Hum.Genet. 55,1:150-159.
Munné S, Lee A, Rosenwaks Z, Grifo J, Cohen J (1993) diagnosis of major chromosome aneuploidies in human preimplantation embryos. Hum Reprod 8:2185-2191
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