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G F Merkx

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Cytogenetics and Cell Genetics|January 1, 1997

Assignment of the canalicular multispecific organic anion transporter gene (CMOAT) to human chromosome 10q24 and mouse chromosome 19D2 by fluorescent in situ hybridizationM A van Kuijck, M Kool, G F Merkx, et al.

Pediatric Nephrology (Berlin, Germany)|August 1, 1996

Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch familiesH H Lemmink, L P van den Heuvel, H A van Dijk, et al.

American Journal of Human Genetics|July 20, 2001

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 13 results.

Cytogenetics and Cell Genetics|January 1, 1997

Pediatric Nephrology (Berlin, Germany)|August 1, 1996

Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch familiesH H Lemmink, L P van den Heuvel, H A van Dijk, et al.

American Journal of Human Genetics|July 20, 2001

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.

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