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Clinical Genetics|October 1, 1990
Possible association of rare autosomal folate sensitive fragile sites and idiopathic mental retardation: a blind controlled population studyA E Chudley, M Ray, J A Evans, et al.Clinical Genetics|October 1, 1990
Autosomal dominant osteopetrosis type II with "malignant" presentation: further support for heterogeneity?I R Walpole, A Nicoll, J GoldblattClinical Genetics|October 1, 1990
Association of hypercholesterolemia and apolipoprotein E4 in school childrenH Yanagi, Y Shimakura, Y Yamanouchi, et al.Clinical Genetics|October 1, 1990
The wrinkly skin syndrome: a report of a case and review of the literatureS A Hurvitz, A Baumgarten, R M GoodmanClinical Genetics|November 26, 2013
Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in IndiaP P Warang, P S Kedar, C Shanmukaiah, et al.Clinical Genetics|November 22, 2012
Knowledge of the Genetic Information Nondiscrimination act among individuals affected by Huntington diseaseE R Dorsey, K C Darwin, P E Nichols, et al.Clinical Genetics|November 21, 2012
Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey studyA A Lemke, D Bick, D Dimmock, et al.Clinical Genetics|November 22, 2012
Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesisA Mostowska, B Biedziak, M Zadurska, et al.Clinical Genetics|September 5, 2015
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosisG Longo, S Russo, G Novelli, et al.Clinical Genetics|July 1, 1989
X-linked myotubular myopathy: clinical and pathological findings in a familyA Oldfors, M Kyllerman, J Wahlström, et al.Pageof 719