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Journal of Medical Genetics|July 1, 1987
Osteogenesis imperfecta type IIA: evidence for dominant inheritanceI D Young, E M Thompson, C M Hall, et al.Journal of Medical Genetics|July 1, 1987
Recurrence risks and prognosis in severe sporadic osteogenesis imperfectaE M Thompson, I D Young, C M Hall, et al.Archives of Disease in Childhood|November 1, 1985
Amniotic bands in connective tissue disordersI D Young, R H Lindenbaum, E M Thompson, et al.Journal of Medical Genetics|November 1, 1991
X linked alpha thalassaemia/mental retardation: spectrum of clinical features in three related malesA O Wilkie, R J Gibbons, D R Higgs, et al.Human Genetics|February 1, 1992
Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndromeJ C Smith, T Webb, M E Pembrey, et al.Health Technology Assessment (Winchester, England)|March 23, 2001
An assessment of screening strategies for fragile X syndrome in the UKM E Pembrey, A J Barnicoat, B Carmichael, et al.Acta Oto-Laryngologica|May 1, 1997
Abnormal audiograms and elevated acoustic reflex thresholds in obligate carriers of autosomal recessive non-syndromic hearing lossM Cohen, M Francis, R Coffey, et al.Current Opinion in Genetics & Development|June 1, 1995
Mapping and cloning hereditary deafness genesF P Cremers, M Bitner-Glindzicz, M E Pembrey, et al.British Journal of Haematology|November 1, 1978
Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi ArabiaM E Pembrey, W G Wood, D J Weatherall, et al.American Journal of Human Genetics|January 1, 1980
Sickle beta 0 thalassemia in Eastern Saudi ArabiaM E Pembrey, R P Perrine, W G Wood, et al.Pageof 23