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M A Crawfurd

Showing results (1-10 of 6) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1982
Review: genetics of steroid sulphatase deficiency and X-linked ichthyosisM A Crawfurd
Journal of Medical Genetics|September 1, 1988
Alport's syndromeM A Crawfurd
BMJ (Clinical Research Ed.)|October 8, 1988
Anderson-Fabry diseaseS H Morgan, M A Crawfurd
British Medical Journal (Clinical Research Ed.)|July 2, 1983
Recognising placental steroid sulphatase deficiencyR A Harkness, N F Taylor, M A Crawfurd, et al.
Pediatric Nephrology (Berlin, Germany)|July 1, 1987
Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probesS H Morgan, J K Cheshire, T M Wilson, et al.
Journal of Medical Genetics|June 1, 1979
Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosisA G Whitelaw, P A Rogers, D A Hopkinson, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of Inherited Metabolic Disease|January 1, 1982
Review: genetics of steroid sulphatase deficiency and X-linked ichthyosisM A Crawfurd
Journal of Medical Genetics|September 1, 1988
Alport's syndromeM A Crawfurd
BMJ (Clinical Research Ed.)|October 8, 1988
Anderson-Fabry diseaseS H Morgan, M A Crawfurd
British Medical Journal (Clinical Research Ed.)|July 2, 1983
Recognising placental steroid sulphatase deficiencyR A Harkness, N F Taylor, M A Crawfurd, et al.
Pediatric Nephrology (Berlin, Germany)|July 1, 1987
Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probesS H Morgan, J K Cheshire, T M Wilson, et al.
Journal of Medical Genetics|June 1, 1979
Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosisA G Whitelaw, P A Rogers, D A Hopkinson, et al.
Pageof 1