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American Journal of Medical Genetics|September 1, 1999
Neurofibromatosis type 1: A model condition for the study of the molecular basis of variable expressivity in human disordersJ C Carey, D H ViskochilBirth Defects Original Article Series|January 1, 1996
Current status of the human malformation mapJ C Carey, D H ViskochilClinical Genetics|March 18, 2006
Clinical and molecular aspects of an informative family with neurofibromatosis type 1 and Noonan phenotypeD A Stevenson, D H Viskochil, A F Rope, et al.Clinical Dysmorphology|January 29, 2000
Wolf-Hirschhorn syndrome (WHS): a history in picturesA Battaglia, J C Carey, D H Viskochil, et al.American Journal of Medical Genetics|February 1, 1990
Congenital hypoplastic (Diamond-Blackfan) anemia in seven members of one kindredD H Viskochil, J C Carey, B E Glader, et al.Pediatrics|April 2, 1999
Natural history of Wolf-Hirschhorn syndrome: experience with 15 casesA Battaglia, J C Carey, P Cederholm, et al.Journal of Musculoskeletal & Neuronal Interactions|June 14, 2005
Case-control study of the muscular compartments and osseous strength in neurofibromatosis type 1 using peripheral quantitative computed tomographyD A Stevenson, L J Moyer-Mileur, J C Carey, et al.American Journal of Medical Genetics|November 14, 2000
Growth failure, intracranial calcifications, acquired pancytopenia, and unusual humoral immunodeficiency: a genetic syndrome?E E Adderson, D H Viskochil, J C Carey, et al.Blood|August 1, 1989
Down-modulation of neutrophil production by erythropoietin in human hematopoietic clonesR D Christensen, J M Koenig, D H Viskochil, et al.Academic Medicine : Journal of the Association of American Medical Colleges|August 5, 2000
Integrating prevention into obstetrics/gynecologyJ C CareyPageof 15