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American Journal of Medical Genetics|August 1, 1985
A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardationM E Pembrey, R M Winter, K E Davies
Lancet (London, England)|July 7, 1984
A clinically useful DNA probe closely linked to haemophilia AK Harper, R M Winter, M E Pembrey, et al.
Bailliere'S Clinical Obstetrics and Gynaecology|September 1, 1987
The impact of DNA analysis on fetal diagnosisM E Pembrey
Journal of Inherited Metabolic Disease|January 1, 1986
Applications and limitations of direct DNA analysis in genetic predictionM E Pembrey
Archives of Disease in Childhood|March 1, 1984
Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophyM E Pembrey, K E Davies, R M Winter, et al.
Journal of Medical Genetics|August 1, 1997
Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome familiesH L Gilbert, J L Buxton, C T Chan, et al.
British Journal of Haematology|April 1, 1983
The estimation of fetal haemoglobin in healthy adults by radioimmunoassayP C Rutland, M E Pembrey, T Davies
Journal of Medical Genetics|February 1, 1985
Trigonocephaly and the Opitz C syndromeC Sargent, J Burn, M Baraitser, et al.
Science (New York, N.Y.)|March 27, 1981
F-cell production in sickle cell anemia: regulation by genes linked to beta-hemoglobin locusG J Dover, S H Boyer, M E Pembrey
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