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F H Fodor

Showing results (1-10 of 4) with videos related to

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Prenatal Diagnosis|March 12, 1999
Molecular exclusion of haemoglobin SD disease by prenatal diagnosisF H Fodor, C M Eng
Nucleic Acids Research|March 11, 1991
A dinucleotide repeat polymorphism at the DMD locusJ F Powell, F H Fodor, D J Cockburn, et al.
Metabolism: Clinical and Experimental|April 1, 1997
Screening for the mitochondrial DNA A3243G mutation in children with insulin-dependent diabetes mellitusM M Abad, P D Cotter, F H Fodor, et al.
American Journal of Human Genetics|June 23, 1998
Frequency and carrier risk associated with common BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer patientsF H Fodor, A Weston, I J Bleiweiss, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Prenatal Diagnosis|March 12, 1999
Molecular exclusion of haemoglobin SD disease by prenatal diagnosisF H Fodor, C M Eng
Nucleic Acids Research|March 11, 1991
A dinucleotide repeat polymorphism at the DMD locusJ F Powell, F H Fodor, D J Cockburn, et al.
Metabolism: Clinical and Experimental|April 1, 1997
Screening for the mitochondrial DNA A3243G mutation in children with insulin-dependent diabetes mellitusM M Abad, P D Cotter, F H Fodor, et al.
American Journal of Human Genetics|June 23, 1998
Frequency and carrier risk associated with common BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer patientsF H Fodor, A Weston, I J Bleiweiss, et al.
Pageof 1