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Annales De Genetique|January 1, 1991
Neuroblastoma in a dwarfed newborn. Possible clue to the chromosomal localization of the gene for achondroplasia?A Verloes, B Massart, V Jossa, et al.Annales De Genetique|January 1, 1991
A triple-X female with long arm deletion of one of the X-chromosomes associated with primary amenorrhoea: 47,XX, +del(X) (q27.3)U Radhakrishna, V C Shah, H N Highland, et al.Annales De Genetique|January 1, 1990
A new DNA probe of potential use for diagnosis of the fragile-X syndromeG LucotteAnnales De Genetique|January 1, 1996
The meiotic pairing behaviour in human spermatocytes carrier of chromosome anomalies and their repercussions on reproductive fitness. II. Robertsonian and reciprocal translocations. A European collaborative studyO Gabriel-Robez, Y RumplerAnnales De Genetique|January 1, 1996
Genetic analysis of genealogies in mentally retarded autistic probands from Saguenay Lac-Saint-Jean (Quebec, Canada)M De Braekeleer, M Tremblay, J ThiviergeAnnales De Genetique|January 1, 1996
De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?M A Redha, D S Krishna Murthy, S A al-Awadi, et al.Annales De Genetique|January 1, 1996
Malformative syndrome with trigonocephaly, shallow orbits, ptosis, growth and mental retardation. De novo autosomal reciprocal t(9;13)(Q32;Q22) in a male patientJ P Fryns, G HendrickxAnnales De Genetique|January 1, 1981
[The karyotypes of Colobus vellersus and of C. palliatus: comparison with Cercopithecidae and man]B Dutrillaux, J Couturier, D RuediAnnales De Genetique|January 1, 1982
[Mechanism of duplication formation relating to a case of 10q22 to q25 duplication]H Pison, B Sele, J Salvat, et al.Annales De Genetique|January 1, 1982
[X chromosome fragility and effects of trimethoprim]J Lejeune, N Legrand, J Lafourcade, et al.Pageof 129