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American Journal of Human Genetics|July 1, 1988
Molecular cytogenetic evidence for amplification of chromosome-specific alphoid sequences at enlarged C-bands on chromosome 6E W Jabs, N CarpenterMolecular Biology & Medicine|August 1, 1990
Characterization of human centromeric regions using restriction enzyme banding, alphoid DNA and structural alterationsP H Arn, E W JabsCell Structure and Function|July 8, 2000
The pleiotropic effects of fibroblast growth factor receptors in mammalian developmentI McIntosh, G A Bellus, E W JabThe British Journal of Dermatology|November 28, 2002
Genes, growth factors and acanthosis nigricansD Torley, G A Bellus, C S MunroCurrent Opinion in Pediatrics|December 1, 1994
Genetics of craniofacial disordersA F Lewanda, E W JabsAmerican Journal of Human Genetics|September 1, 1987
Characterization of human centromeric regions of specific chromosomes by means of alphoid DNA sequencesE W Jabs, M G PersicoClinical Genetics|June 14, 2000
Online Mendelian Inheritance in Man (OMIM) as a knowledgebase for human developmental disordersS A Boyadjiev, E W JabsHuman Molecular Genetics|July 1, 1995
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variabilityW J Park, G A Meyers, X Li, et al.American Journal of Medical Genetics|June 22, 1999
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3G A Bellus, M J Bamshad, K A Przylepa, et al.American Journal of Human Genetics|August 1, 1995
Analysis of phenotypic features and FGFR2 mutations in Apert syndromeW J Park, C Theda, N E Maestri, et al.Pageof 24