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Developmental Medicine and Child Neurology|February 12, 1998
Retesting for fragile X syndrome in cytogenetically normal malesP Gringras, A BarnicoatJournal of Intellectual Disability Research : JIDR|March 24, 1999
Diagnosis of fragile-X syndrome: the experiences of parentsB Carmichael, M Pembrey, G Turner, et al.Clinical Dysmorphology|October 1, 1996
A distinctive overgrowth syndrome with polysyndactylyA Barnicoat, M Salman, L Chitty, et al.Human Genetics|January 27, 2000
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bpK Buiting, C Lich, S Cottrell, et al.American Journal of Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.Clinical Dysmorphology|July 12, 2001
Joint and skin laxity with Dandy-Walker malformation and contractures: a distinct recessive syndrome?S A McKee, A Barnicoat, A Fryer, et al.Lancet (London, England)|October 23, 1993
Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndromeQ Wang, E Green, A Barnicoat, et al.Human Genetics|June 21, 2001
Oto-facio-cervical (OFC) syndrome is a contiguous gene deletion syndrome involving EYA1: molecular analysis confirms allelism with BOR syndrome and further narrows the Duane syndrome critical region to 1 cMS Rickard, M Parker, W van't Hoff, et al.Human Molecular Genetics|February 1, 1993
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXEM C Hirst, A Barnicoat, G Flynn, et al.American Journal of Human Genetics|August 1, 1994
A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 casesF Rousseau, D Heitz, J Tarleton, et al.Pageof 2