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D B Gould

Showing results (31-40 of 33) with videos related to

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European Journal of Human Genetics : EJHG|March 14, 2000
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25F Mirzayans, D B Gould, E Héon, et al.
Journal of Medical Genetics|August 19, 2005
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephalyG Breedveld, I F de Coo, M H Lequin, et al.
American Journal of Human Genetics|October 30, 1998
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomalyA J Mears, T Jordan, F Mirzayans, et al.
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Showing results (31-40 of 33) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 33 results.
European Journal of Human Genetics : EJHG|March 14, 2000
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25F Mirzayans, D B Gould, E Héon, et al.
Journal of Medical Genetics|August 19, 2005
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephalyG Breedveld, I F de Coo, M H Lequin, et al.
American Journal of Human Genetics|October 30, 1998
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomalyA J Mears, T Jordan, F Mirzayans, et al.
Pageof 4