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R L Touraine

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Gynecologie, Obstetrique & Fertilite|January 23, 2004
[A simple, low-cost and non-invasive method for screening Y microdeletions in infertile men]I Aknin-Seifer, R-L Touraine, H Lejeune, et al.
Human Reproduction (Oxford, England)|February 7, 2003
A simple, low cost and non-invasive method for screening Y-chromosome microdeletions in infertile menI E Aknin-Seifer, R L Touraine, H Lejeune, et al.
Human Reproduction (Oxford, England)|January 15, 2005
Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French studyI E Aknin-Seifer, R L Touraine, H Lejeune, et al.
American Journal of Human Genetics|April 14, 2000
Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brainR L Touraine, T Attié-Bitach, E Manceau, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasiaE Mornet, A Taillandier, S Peyramaure, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Gynecologie, Obstetrique & Fertilite|January 23, 2004
[A simple, low-cost and non-invasive method for screening Y microdeletions in infertile men]I Aknin-Seifer, R-L Touraine, H Lejeune, et al.
Human Reproduction (Oxford, England)|February 7, 2003
A simple, low cost and non-invasive method for screening Y-chromosome microdeletions in infertile menI E Aknin-Seifer, R L Touraine, H Lejeune, et al.
Human Reproduction (Oxford, England)|January 15, 2005
Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French studyI E Aknin-Seifer, R L Touraine, H Lejeune, et al.
American Journal of Human Genetics|April 14, 2000
Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brainR L Touraine, T Attié-Bitach, E Manceau, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasiaE Mornet, A Taillandier, S Peyramaure, et al.
Pageof 2