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Clinical Genetics|May 1, 1996
Bloom's syndrome. XIX. Cytogenetic and population evidence for genetic heterogeneityJ German, N A Ellis, M ProytchevaClinical Genetics|May 1, 1996
Sex reversal in a child with the karyotype 46,XY, dup (1) (p22.3p32.3)P Wieacker, D Missbach, S Jakubiczka, et al.Clinical Genetics|December 1, 1995
Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO geneF Blanquet-Grossard, D Pham-Dinh, A Dautigny, et al.Clinical Genetics|December 1, 1995
Association between a dimorphic site on chromosome 12 and clinical diagnosis of hypertension in three independent populationsP M Frossard, G G LestringantClinical Genetics|December 1, 1995
Increased frequency of apolipoprotein epsilon 2 allele in non-insulin dependent diabetic (NIDDM) patients with nephropathyM Eto, K Horita, A Morikawa, et al.Clinical Genetics|December 1, 1995
Common genetic variants of lipoprotein lipase that relate to lipid transport in patients with premature coronary artery diseaseQ Zhang, J Cavanna, B R Winkelman, et al.Clinical Genetics|December 1, 1995
Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancerJ A Joyce, N J Froggatt, R Davies, et al.Clinical Genetics|December 1, 1995
Trisomy 1 mosaicism only detected on a direct chromosome preparation in a neonateP J Howard, C E Cramp, A E FryerClinical Genetics|December 1, 1995
Two brothers with an unbalanced 8;17 translocation and infantile pyloric stenosisS V Hodgson, A C Berry, H M DunbarClinical Genetics|February 1, 1997
Mutation of RET codon 768 is associated with the FMTC phenotypeL M Boccia, J S Green, C Joyce, et al.Pageof 719