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Gene|March 9, 1996
The human S3a ribosomal protein: sequence, location and cell-free transcription of the functional geneD Nolte, G Taimor, M Kalff-Suske, et al.American Journal of Medical Genetics|March 4, 2000
Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individualD Sobetzko, G Eich, M Kalff-Suske, et al.Annals of the New York Academy of Sciences|February 24, 2001
All human genes of the uteroglobin family are localized on chromosome 11q12.2 and form a dense clusterJ Ni, M Kalff-Suske, R Gentz, et al.Genomics|June 1, 1993
All known human H1 histone genes except the H1(0) gene are clustered on chromosome 6W Albig, B Drabent, J Kunz, et al.Human Molecular Genetics|September 25, 1997
Point mutations in human GLI3 cause Greig syndromeA Wild, M Kalff-Suske, A Vortkamp, et al.Clinical Genetics|March 31, 1998
Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormalityP G Williams, J H Hersh, F F Yen, et al.Genomics|July 15, 1994
Regional localization of 725 human chromosome 7-specific yeast artificial chromosome clonesJ Kunz, S W Scherer, I Klawitz, et al.The Journal of Biological Chemistry|December 6, 1996
Molecular characterization of human zyxinT Macalma, J Otte, M E Hensler, et al.American Journal of Medical Genetics. Part A|June 10, 2003
Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutationsPhilippe Debeer, H Peeters, S Driess, et al.Human Molecular Genetics|August 11, 1999
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndromeM Kalff-Suske, A Wild, J Topp, et al.Pageof 1