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Lancet (London, England)|April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiencyJ Goodship, S Malcolm, Y L Lau, et al.British Medical Journal|July 21, 1973
Thalassaemia in the BritishH H Knox-Macaulay, D J Weatherall, J B Clegg, et al.Journal of Medical Genetics|February 1, 1997
Pendred syndrome: evidence for genetic homogeneity and further refinement of linkageE Gausden, B Coyle, J A Armour, et al.Journal of Medical Genetics|June 1, 1993
Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndromeJ Clayton-Smith, T Webb, X J Cheng, et al.British Journal of Haematology|February 1, 1975
Haemoglobin Bart's in Saudi ArabiaM E Pembrey, D J Weatherall, J B Clegg, et al.Molecular Medicine Today|December 1, 1995
The molecular pathology of syndromic craniosynostosisW Reardon, R M WinterEuropean Journal of Human Genetics : EJHG|January 1, 1993
Syndactylies and polydactylies: embryological overview and suggested classificationR M Winter, C TickleJournal of Medical Genetics|July 1, 1989
Disorganisation: a model for 'early amnion rupture'?D Donnai, R M WinterJournal of Medical Genetics|August 1, 1981
Hydrocephalus, agyria, pseudoencephalocele, retinal dysplasia, and anterior chamber anomaliesR M Winter, A GarnerJournal of Medical Genetics|July 1, 1989
Kyphomelic dysplasiaI K Temple, E M Thompson, C M Hall, et al.Pageof 23