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P W Lunt

Showing results (41-50 of 44) with videos related to

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British Medical Journal (Clinical Research Ed.)|November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.
Journal of Medical Genetics|September 8, 2001
Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolismA L Kelly, P W Lunt, F Rodrigues, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
The Opitz syndrome gene product, MID1, associates with microtubulesS Schweiger, J Foerster, T Lehmann, et al.
Human Molecular Genetics|January 1, 1997
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2M Oldridge, P W Lunt, E H Zackai, et al.
Pageof 5

Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
British Medical Journal (Clinical Research Ed.)|November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.
Journal of Medical Genetics|September 8, 2001
Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolismA L Kelly, P W Lunt, F Rodrigues, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
The Opitz syndrome gene product, MID1, associates with microtubulesS Schweiger, J Foerster, T Lehmann, et al.
Human Molecular Genetics|January 1, 1997
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2M Oldridge, P W Lunt, E H Zackai, et al.
Pageof 5