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American Journal of Medical Genetics|January 10, 1997
Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisationP J Morrison, N M Smith, K E Martin, et al.Journal of Intellectual Disability Research : JIDR|February 1, 1995
Long-term survival in the Wolf-Hirschhorn (4p-) syndromeS A Smith, A M Walker, A J Monk, et al.Clinical Dysmorphology|August 5, 1998
Distal arthrogryposis, ectodermal dysplasia and dilated cardiomyopathy--a new syndrome?M J Parker, R C Groggins, P G Rees, et al.Journal of Medical Genetics|July 1, 1987
Osteogenesis imperfecta type IIA: evidence for dominant inheritanceI D Young, E M Thompson, C M Hall, et al.Journal of Medical Genetics|July 1, 1987
Recurrence risks and prognosis in severe sporadic osteogenesis imperfectaE M Thompson, I D Young, C M Hall, et al.Archives of Disease in Childhood|November 1, 1985
Amniotic bands in connective tissue disordersI D Young, R H Lindenbaum, E M Thompson, et al.Journal of Medical Genetics|October 1, 1993
Sex linked valvular dysplasiaR A Newbury-Ecob, J M Zuccollo, N Rutter, et al.Ophthalmic Paediatrics and Genetics|March 1, 1990
Ocular findings in Angelman's (happy puppet) syndromeA J Dickinson, A R Fielder, I D Young, et al.Journal of Medical Genetics|June 1, 1989
Prenatal diagnosis of the megacystis-microcolon-intestinal hypoperistalsis syndromeI D Young, P A McKeever, L A Brown, et al.Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|May 1, 1993
Synthesis of digoxigenin-labeled cRNA probes for nonisotopic in situ hybridization using reverse transcription polymerase chain reactionI D Young, R J Stewart, L Ailles, et al.Pageof 104