Chromosome analysis of human spermatozoa stored in vitroMUNNE, S; ESTOP, A. M.Human reproduction (Oxford. Print). 1993, Vol 8, Num 4, pp 581-586, issn 0268-1161Article

The effect of in-vitro ageing on mouse sperm chromosomesMUNNE, S; ESTOP, A.Human reproduction (Oxford. Print). 1991, Vol 6, Num 5, pp 703-708, issn 0268-1161Article

CONSTITUTIVE HETEROCHROMATIN POLYMORPHISM IN LAGOTHRIX LAGOTHRICHA CANA, CEBUS APELLA, AND CEBUS CAPUCINUSGARCIA M; MIRO R; ESTOP A et al.1983; AMERICAN JOURNAL OF PRIMATOLOGY; ISSN 0275-2565; USA; DA. 1983; VOL. 4; NO 2; PP. 117-126; BIBL. 2 P.Article

Duplication 20p identified via fluorescent in situ hybridizationLECHIEN, K. A; MCPHERSON, E; ESTOP, A. M et al.American journal of medical genetics. 1994, Vol 50, Num 2, pp 187-189, issn 0148-7299Article

The genotoxic effect of β-propiolactone on mammalian oocytesSANTALO, J; ESTOP, A. M; EGOZCUE, J et al.Mutation research. 1987, Vol 189, Num 4, pp 407-416, issn 0027-5107Article

Preimplantation Genetic Diagnosis for Complex Chromosome RearrangementsESCUDERO, T; ESTOP, A; FISCHER, J et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 13, pp 1662-1669, issn 1552-4825, 8 p.Article

The chromosome complement of first-cleavage mouse embryos after in vitro fertilizationSANTALO, J; ESTOP, A. M; EGOZCUE, J et al.Journal of in vitro fertilization and embryo transfer. 1986, Vol 3, Num 2, pp 99-105, issn 0740-7769Article

Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)ESTOP, A. M; CIEPLY, K. M; MUNNE, S et al.Human genetics. 1999, Vol 104, Num 5, pp 412-417, issn 0340-6717Article

Sexual immaturity and maternal age: incidence of aneuploidy and polyploidy in first-cleavage mouse embryosCATALA, V; ESTOP, A. M; SANTALO, J et al.Cytogenetics and cell genetics. 1988, Vol 48, Num 4, pp 233-237, issn 0301-0171Article

The segregation of a translocation t(3;4) in two male carriers heterozygous for the translocationESTOP, A. M; LEVINSON, F; CIEPLY, K et al.Human genetics. 1992, Vol 89, Num 4, pp 425-429, issn 0340-6717Article

Studies on sperm chromatin structure alterations and cytogenetic damage of mouse sperm following in vitro incubation. Studies on in vitro-incubated mouse spermESTOP, A. M; MUNNE, S; JOST, L. K et al.Journal of andrology. 1993, Vol 14, Num 4, pp 282-288, issn 0196-3635Article

Cytogenetic studies in human spermESTOP, A. M; CIEPLY, K; VANKIRK, V et al.Human genetics. 1991, Vol 87, Num 4, pp 447-451, issn 0340-6717Article

Effect of the degree of maturation of mouse oocytes at fertilization: a source of chromosome imbalanceBADENAS, J; SANTALO, J; CALAFELL, J. M et al.Gamete research. 1989, Vol 24, Num 2, pp 205-218, issn 0148-7280Article

Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysisESTOP, A. M; MUNNE, S; CIEPLY, K. M et al.Human reproduction (Oxford. Print). 1998, Vol 13, Num 1, pp 124-127, issn 0268-1161Article

Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypesESTOP, A. M; BANSAL, V; LIN, A et al.American journal of medical genetics. 1994, Vol 49, Num 4, pp 410-413, issn 0148-7299Article

The genetic risks of in vitro fertilization techniques: the use of an animal modelSANTALO, J; BADENAS, J; CALAFELL, J. M et al.Journal of assisted reproduction and genetics. 1992, Vol 9, Num 5, pp 462-474Article

A Ph-negative chronic myeloid leukemia patient with a non-classical BCR-ABL rearrangement characterized by fluorescence in situ hybridizationESTOP, A. M; SHERER, C; CIEPLY, K et al.Cancer genetics and cytogenetics. 1997, Vol 96, Num 2, pp 174-176, issn 0165-4608Article

Segregation analysis of four translocations, t(2;18), t(3;15), t(5;7), and t(10;12), by sperm chromosome studies and a review of the literatureESTOP, A. M; VAN KIRK, V; CIEPLY, K et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 80-87, issn 0301-0171Conference Paper

Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic featuresESTOP, A. M; MOWERY-RUSHTON, P. A; CIEPLY, K. M et al.Journal of medical genetics. 1995, Vol 32, Num 10, pp 819-822, issn 0022-2593Article

An analysis of human sperm chromosome breakpointsESTOP, A. M; MARQUEZ, C; MUNNE, S et al.American journal of human genetics. 1995, Vol 56, Num 2, pp 452-460, issn 0002-9297Article

An analysis of human sperm chromosome aneuploidyTEMPLADO, C; MARQUEZ, C; MUNNE, S et al.Cytogenetics and cell genetics. 1996, Vol 74, Num 3, pp 194-200, issn 0301-0171Conference Paper