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Clinical Genetics|October 1, 1996
Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26)T Tsukuda, I Nagata, H Sawada, et al.Clinical Genetics|October 1, 1996
A case report of 46,XX,del(21)(q22) de novo deletion associated with Imerslund-Grasbeck syndromeF Celep, A Karagüzel, F M Aynaci, et al.Clinical Genetics|October 1, 1996
Further evidence for a syndrome of "apple peel" intestinal atresia, ocular anomalies and microcephalyJ Slee, J GoldblattClinical Genetics|October 1, 1996
Mild form of beta-ketothiolase deficiency (mitochondrial acetoacetyl-CoA thiolase deficiency) in two Japanese siblings: identification of detectable residual activity and cross-reactive material in EB-transformed lymphocytesT Fukao, A Kodama, N Aoyanagi, et al.Clinical Genetics|January 1, 1979
Human gene mapping by postreduction and recombination frequencies under complete interferenceJ OttClinical Genetics|April 1, 1995
Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosisA Pekrun, B A Neubauer, S W Eber, et al.Clinical Genetics|April 1, 1995
Familial hypertryptophanemia in two siblingsJ R Martin, C S Mellor, F C FraserClinical Genetics|April 1, 1995
Restriction fragment length polymorphisms at the apoprotein genes AI, CIII and B-100 and in the 5' flanking region of the insulin gene as possible markers of coronary heart diseaseU Wick, E Witt, W EngelClinical Genetics|October 7, 1998
Spinal and bulbar muscular atrophy (SBMA): somatic stability of an expanded CAG repeat in fetal tissuesK B Jedele, D Wahl, S Chahrokh-Zadeh, et al.Pageof 719