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Genomics|June 15, 1999
A complete physical contig and partial transcript map of the Williams syndrome critical regionE L Hockenhull, M J Carette, K Metcalfe, et al.Human Molecular Genetics|July 1, 1997
Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosisM Tassabehji, K Metcalfe, D Donnai, et al.American Journal of Medical Genetics|July 1, 1993
NICHD conference. Robertsonian translocations: clues to imprintingD DonnaiAmerican Journal of Medical Genetics|May 1, 1986
A further patient with the Pitt-Rogers-Danks syndrome of mental retardation, unusual face, and intrauterine growth retardationD DonnaiBailliere'S Clinical Obstetrics and Gynaecology|September 1, 1987
The management of the patient having fetal diagnosisD DonnaiHuman Molecular Genetics|June 13, 1998
An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxaM Tassabehji, K Metcalfe, J Hurst, et al.American Journal of Medical Genetics|October 1, 1993
Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?D Donnai, M BarrowClinical Dysmorphology|April 18, 1998
A boy with severe manifestations of type A1 brachydactylyA Slavotinek, D DonnaiPageof 19