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Annals of Human Genetics|May 1, 1975
Segregation of ACP1 and MNSs in families with structural rearrangements involving chromosome 2M A Mace, J Noades, E B Robson, et al.Journal of Medical Genetics|June 1, 1989
Unknown syndrome: congenital heart disease, choanal stenosis, short stature, developmental delay, and dysmorphic facial features in a brother and sisterJ A Hurst, A C Berry, M A TettenbornClinical Genetics|December 1, 1995
Two brothers with an unbalanced 8;17 translocation and infantile pyloric stenosisS V Hodgson, A C Berry, H M DunbarJournal of Medical Genetics|April 1, 1987
A child with partial monosomy 6q secondary to a maternal direct insertional eventS V Matkins, J E Meyer, A C BerryActa Paediatrica (Oslo, Norway : 1992)|March 24, 1998
FISH analysis in patients with clinical diagnosis of Williams syndromeN Elçioglu, C Mackie-Ogilvie, M Daker, et al.Journal of Medical Genetics|February 1, 1990
Yunis-Varon syndrome with severe osteodysplastyC Garrett, A C Berry, R H Simpson, et al.Prenatal Diagnosis|November 1, 1989
Prenatal diagnosis of a case of tetrasomy 9pA A McDowall, S Blunt, A C Berry, et al.Clinical Genetics|January 1, 1997
Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigationF Behjati, M Mullarkey, A Bergbaum, et al.Journal of Medical Genetics|June 1, 1977
Prenatal recognition of 4p- syndromeS Blunt, A C Berry, M J Seller, et al.Journal of Medical Genetics|August 1, 1992
Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidismM M Lai, P N Scriven, C Ball, et al.Pageof 7