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Lancet (London, England)|August 10, 1999
Left-isomerism sequence and maternal type-1 diabetesM Splitt, C Wright, D Sen, et al.American Journal of Human Genetics|July 13, 2000
Autozygosity mapping of a seckel syndrome locus to chromosome 3q22. 1-q24J Goodship, H Gill, J Carter, et al.Prenatal Diagnosis|August 1, 1995
A case of paternal uniparental disomy for chromosome 11A Webb, J Beard, C Wright, et al.Prenatal Diagnosis|October 8, 1997
Renal abnormalities on obstetric ultrasound as a presentation of DiGeorge syndromeJ Goodship, S C Robson, S Sturgiss, et al.Clinical Dysmorphology|January 11, 2001
A family with distal arthrogryposis and cleft palate: possible overlap between Gordon syndrome and Aase-Smith syndromeK Becker, M SplittCurrent Opinion in Genetics & Development|June 1, 1996
Developmental genetics of the heartJ Burn, J GoodshipKidney International|July 1, 2006
Factor H genotype-phenotype correlations: lessons from aHUS, MPGN II, and AMDT H J GoodshipCurrent Opinion in Hematology|July 9, 2010
Atypical hemolytic uremic syndromeDavid Kavanagh, Timothy H J GoodshipHuman Genetics|December 1, 1989
Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving maleJ Goodship, R Levinsky, S MalcolmSeminars in Thrombosis and Hemostasis|April 1, 2006
Membrane cofactor protein and factor I: mutations and transplantationDavid Kavanagh, Timothy H J GoodshipPageof 391