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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2001
Heterotaxy: associated conditions and hospital-based prevalence in newbornsA E Lin, B S Ticho, K Houde, et al.Journal of Medical Genetics|November 1, 1995
Absence/hypoplasia of tibia, polydactyly, retrocerebellar arachnoid cyst, and other anomalies: an autosomal recessive disorderL B Holmes, R W Redline, D L Brown, et al.American Journal of Medical Genetics|August 1, 1984
Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndromeS Kitsiou-Tzeli, J J Hallett, L Atkins, et al.Teratology|March 1, 1994
Anticonvulsant teratogenesis: I. A study design for newborn infantsL B Holmes, E A Harvey, K S Brown, et al.American Journal of Medical Genetics|March 7, 1998
New syndrome? Prominent, constricted ears with malformed condyle of the mandibleM Jampol, G Repetto, D A Keith, et al.Blood|December 1, 1985
Leukemia with Down's syndrome: translocation between chromosomes 1 and 19 in acute myelomonocytic leukemia following transient congenital myeloproliferative syndromeR Morgan, F Hecht, M L Cleary, et al.Birth Defects Original Article Series|January 1, 1976
Human centromere mapping using teratoma dataJ Ott, F Hecht, D Linder, et al.Blood|March 1, 1986
Cytogenetic and immunophenotypic analysis of cell lines established from patients with T cell leukemia/lymphomaS D Smith, R Morgan, M P Link, et al.The American Journal of Medicine|June 1, 1984
Chromosome analysis in hematologic disorders. The leukemiasA A Sandberg, R Morgan, C Berger, et al.Clinical Genetics|March 1, 1986
Genetic control over fragile X chromosome expressionF Hecht, J P Fryns, R F Vlietinck, et al.Pageof 26