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Molecular Genetics and Metabolism|October 21, 1999
Molecular mechanisms of holoprosencephalyD E Wallis, M MuenkeCurrent Opinion in Genetics & Development|May 29, 2000
Genetics of ventral forebrain development and holoprosencephalyM Muenke, P A BeachyHuman Genetics|August 2, 2001
Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephalyI M Orioli, E E Castilla, J E Ming, et al.Human Genetics|July 8, 1999
Analysis of the mutational spectrum of the FGFR2 gene in Pfeiffer syndromeL R Cornejo-Roldan, E Roessler, M MuenkeAmerican Journal of Medical Genetics|March 15, 1996
Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toesN H Robin, B Segel, G Carpenter, et al.Genomics|January 1, 1993
Regional assignment of the human homeobox-containing gene EN1 to chromosome 2q13-q21A Köhler, C Logan, A L Joyner, et al.Molecular Genetics and Metabolism|July 31, 1998
Analysis of patients with craniosynostosis syndromes for a pro246Arg mutation of FGFR4K Gaudenz, E Roessler, S Vainikka, et al.Archives of Disease in Childhood|March 29, 2002
Extreme variability of expression of a Sonic Hedgehog mutation: attention difficulties and holoprosencephalyH S Heussler, M Suri, I D Young, et al.American Journal of Medical Genetics|March 10, 2000
Holoprosencephaly: molecular study of a California populationL Nanni, L A Croen, E J Lammer, et al.Pageof 12