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American Journal of Medical Genetics|July 31, 1995
Identical twins with Cohen syndromeK N North, A B Fulton, D A WhitemanAmerican Journal of Medical Genetics|January 2, 1996
Treacher Collins syndrome: phenotypic variability in a family including an infant with arhinia and uveal colobomasM Hansen, M J Lucarelli, D A Whiteman, et al.Annals of Neurology|December 1, 1995
Cerebrovascular complications in Ehlers-Danlos syndrome type IVK N North, D A Whiteman, M G Pepin, et al.Clinical Genetics|February 1, 1991
Brief clinical report: a 46,XY phenotypic female with Smith-Lemli-Opitz syndromeM F Lachman, Y Wright, D A Whiteman, et al.American Journal of Medical Genetics|July 17, 1995
CHARGE association in a child with de novo inverted duplication (14)(q22-->q24.3)K N North, B L Wu, B N Cao, et al.American Journal of Medical Genetics|September 15, 1991
Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2D J Aughton, S B Cassidy, D A Whiteman, et al.Human Genetics|July 1, 1986
The human ribosomal RNA genes: structure and organization of the complete repeating unitJ E Sylvester, D A Whiteman, R Podolsky, et al.Journal of Inherited Metabolic Disease|December 22, 1999
Hypoglycinaemia and psychomotor delay in a child with xeroderma pigmentosumE J Quackenbush, K H Kraemer, W A Gahl, et al.American Journal of Medical Genetics|December 1, 1991
Mucolipidosis type IV: clinical manifestations and natural historyD Chitayat, C M Meunier, K A Hodgkinson, et al.Human Molecular Genetics|May 1, 1993
Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprintedR Weksberg, I Teshima, B R Williams, et al.Pageof 1