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Clinical Dysmorphology|April 1, 1992
Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3D Donnai, L J Heather, P Sinclair, et al.Journal of Medical Genetics|December 1, 1987
Multiple pterygium syndrome: evolution of the phenotypeE M Thompson, D Donnai, M Baraitser, et al.Human Molecular Genetics|August 15, 2000
The Conradi-Hünermann-Happle syndrome (CDPX2) and emopamil binding protein: novel mutations, and somatic and gonadal mosaicismC Has, L Bruckner-Tuderman, D Müller, et al.American Journal of Medical Genetics|August 1, 1993
True telomeric translocation in a baby with the Prader-Willi phenotypeA Reeve, A Norman, P Sinclair, et al.Journal of Medical Genetics|November 1, 1996
Rothmund-Thomson syndrome: two case reports show heterogeneous cutaneous abnormalities, an association with genetically programmed ageing changes, and increased chromosomal radiosensitivityB Kerr, G S Ashcroft, D Scott, et al.American Journal of Medical Genetics|April 10, 1995
Prenatal diagnosis of Smith-Lemli-Opitz syndromeJ M McGaughran, P T Clayton, K A Mills, et al.The Quarterly Journal of Medicine|August 1, 1992
A clinical study of type 2 neurofibromatosisD G Evans, S M Huson, D Donnai, et al.International Journal of Pancreatology : Official Journal of the International Association of Pancreatology|January 1, 1988
Chronic pancreatitis, HLA and autoimmunityR J Anderson, P A Dyer, D Donnai, et al.American Journal of Human Genetics|June 1, 1990
Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouseC Foy, V Newton, D Wellesley, et al.Journal of Medical Genetics|March 1, 1990
Cranial hemihypertrophy and neurodevelopmental prognosisJ C Dean, G F Cole, R E Appleton, et al.Pageof 19