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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 ViskochilBlood|August 1, 1989
Down-modulation of neutrophil production by erythropoietin in human hematopoietic clonesR D Christensen, J M Koenig, D H Viskochil, et al.Clinical 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 Medical Genetics|January 7, 2009
Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1J J Swensen, J Keyser, C M Coffin, et al.The Journal of Biological Chemistry|July 25, 1983
Isolation of two genomic sequences encoding the Mr = 14,000 subunit of rat prostateinD H Viskochil, S T Perry, O A Lea, 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.Pageof 3