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Garcia-Esquivel L

Mexican Social Security Institute

12

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78

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Cortical blindness, growth and psychomotor retardation and postaxial Polydactyly: A probably distinct autosomal recessive syndrome

2008 Clinical Genetics
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Centric fission, centromere‐telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy

2008 Clinical Genetics
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Inv(4)(p16q21). A five‐generation pedigree with 24 carriers and no recombin ants

2008 Clinical Genetics
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De novo inv(5)(p15q22), del(5)(p15) in a boy with cri du chat syndrome.

1987 Journal of Medical Genetics
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Familial trisomy 3q25→qter. Report of two cases

1987 Journal de génétique humaine
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Cytogenetic evaluation of 163 azoospermics

1987 Journal de génétique humaine
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Ciliary and superciliary hypotrichosis a distinct autosomal dominant trait

1986 Ophthalmic Genetics
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De novo del(7)(pter----p21.2::p15.2----qter) and craniosynostosis. Implications for critical segment assignment in the 7p2 monosomy syndrome.

1986 Annales De Genetique
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Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.

1985 Annales De Genetique
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Citations (3)