Showing results (731-740 of 7,173) with videos related to
Sort By:
Pageof 718
Clinical Genetics|August 14, 2018
Genetic regulatory pathways of split-hand/foot malformationPiranit N Kantaputra, Bruce M CarlsonClinical Genetics|September 1, 1985
I-cell disease: clinical studies of 21 Japanese casesS Okada, M Owada, T Sakiyama, et al.Clinical Genetics|April 28, 2018
Refining the phenotype associated with biallelic DNAJC21 mutationsG D'Amours, F Lopes, J Gauthier, et al.Clinical Genetics|May 4, 2018
EAST/SeSAME syndrome: Review of the literature and introduction of four new Latvian patientsM Celmina, I Micule, I Inashkina, et al.Clinical Genetics|April 3, 1999
Evaluation of the facioscapulohumeral muscular dystrophy (FSHD1) phenotype in correlation to the concurrence of 4q35 and 10q26 fragmentsJ Köhler, D Röhrig, K D Bathke, et al.Clinical Genetics|April 3, 1999
Antibody deficiency, growth retardation, spondyloepiphyseal dysplasia and retinal dystrophy: a novel syndromeC M RoifmanClinical Genetics|April 3, 1999
Alternative splicing of exon 37 of FBN1 deletes part of an 'eight-cysteine' domain resulting in the Marfan syndromeJ McGrory, W G ColeClinical Genetics|June 11, 1999
A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysisA Paoloni-Giacobino, M H Dutoit, M A Morris, et al.Clinical Genetics|June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.Clinical Genetics|January 1, 1976
Infantile polymyoclonus: Its occurrence in second cousinsG C Robinson, J E Jan, H G DunnPageof 718