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Journal De Genetique Humaine|August 1, 1987
Familial trisomy 3q25----qter. Report of two casesL Garcia-Esquivel, F Rivas, H Rivera, et al.Journal De Genetique Humaine|August 1, 1987
inv(5)(p13q13) in a four generation pedigreeE Vargas-Moyeda, H Rivera, D Garcia-Cruz, et al.Journal De Genetique Humaine|October 1, 1975
[The incidence of constitutional chromosome aberrations]R BergerJournal De Genetique Humaine|October 1, 1975
Cytochemistry of cultured fibroblasts in myotonic muscular dystrophyF Lo Curto, A Castello, U Magrini, et al.Journal De Genetique Humaine|October 1, 1975
[Studies of the mitotic and meiotic chromosomes in infertile males]L Koulischer, R SchoysmanJournal De Genetique Humaine|October 1, 1975
[Epidemiological aspects of trisomy 21]F Giraud, J F MatteiJournal De Genetique Humaine|October 1, 1975
[Chromosome analyses in parents of children with trisomy 21[]J F Mattei, F GiraudJournal De Genetique Humaine|January 1, 1988
[Major malformation syndrome and apparently balanced chromosomal abnormality: holoprosencephaly and 5p; 12q translocation]J Cousin, C Creusy, M F Croquette, et al.Journal De Genetique Humaine|December 1, 1987
[Fatal multiple pterygium syndrome and nuchal hygroma]F Serville, B Maugey, D Carles, et al.Journal De Genetique Humaine|May 1, 1987
[Second prenatal diagnosis in a familial form of male pseudohermaphroditism caused by 17 keto-reductase deficiency: prediction confirmed by a normal third male infant]J L Nivelon, M G Forest, A Nivelon-Chevallier, et al.Pageof 47