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Current Opinion in Pediatrics|December 1, 1994
Genetics of craniofacial disordersA F Lewanda, E W JabsAmerican Journal of Medical Genetics|November 6, 1995
Two craniosynostotic patients with 11q deletions, and review of 48 casesA F Lewanda, S Morsey, C S Reid, et al.American Journal of Diseases of Children (1960)|December 1, 1993
Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorderA F Lewanda, M M Cohen, J Hood, et al.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 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 JabsAmerican Journal of Medical Genetics|June 15, 1993
Mild mandibulofacial dysostosis in a child with a deletion of 3pP H Arn, C Mankinen, E W JabsProceedings of the National Academy of Sciences of the United States of America|August 1, 1984
Characterization of a cloned DNA sequence that is present at centromeres of all human autosomes and the X chromosome and shows polymorphic variationE W Jabs, S F Wolf, B R MigeonDevelopmental Medicine and Child Neurology|June 1, 1992
Roberts/pseudothalidomide syndrome and normal intelligence: approaches to diagnosis and managementK R Holden, E W Jabs, P D SponsellerPageof 11