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American Journal of Medical Genetics|March 29, 1996
Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextropositionA D Irvine, F J Stewart, E A Bingham, et al.American Journal of Medical Genetics|February 15, 1993
Axial mesodermal dysplasia spectrumF J Stewart, N C Nevin, S BrownClinical Genetics|August 1, 1994
Microcephaly with large anterior fontanelle, generalized convulsions, micropenis, and distinct anomalies of the hands and feet. Another example of Wiedemann syndrome?N C Nevin, F J Stewart, C W Corkey, et al.Human Mutation|January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosisJ Zschocke, C A Graham, F J Stewart, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemiaJ Zschocke, C A Graham, F J Stewart, et al.Clinical Genetics|March 1, 1996
Wolcott-Rallison syndrome associated with congenital malformations and a mosaic deletion 15q 11-12F J Stewart, D J Carson, P S Thomas, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
Prevention and avoidance of congenital malformationsN C NevinAnnals of the New York Academy of Sciences|February 3, 1999
Experience of gene therapy in the United KingdomN C NevinJournal of Medical Genetics|November 1, 1996
An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalisA D Irvine, O M Dolan, D R Hadden, et al.BJU International|February 13, 2003
Glanular reconstruction and preputioplasty repair for distal hypospadias: a unique day-case method to avoid urethral stenting and preserve the prepuceJ Gray, V E BostonPageof 19