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A F Roux

Showing results (1-10 of 24) with videos related to

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Journal Francais D'Ophtalmologie|March 16, 2005
[Molecular updates on Usher syndrome]A-F Roux
Methods in Enzymology|January 1, 1988
Alpha 1-acid glycoproteinP Arnaud, L Miribel, A F Roux
Cytogenetics and Cell Genetics|July 15, 2000
Genomic sequencing reveals the structure of the Kcnk6 and map3k11 genes and their close vicinity to the sipa1 gene on mouse chromosome 19A Saridaki, C Ferraz, J Demaille, et al.
Human Molecular Genetics|October 1, 1994
A heat shock gene at 14q22: mapping and expressionA F Roux, V T Nguyen, J A Squire, et al.
Human Molecular Genetics|June 1, 1993
Dinucleotide repeat polymorphism near the RP3 locus in Xp21 (DXS1110)A F Roux, C C Yuan, J M Rommens, et al.
Genomics|July 15, 1997
Physical and transcription map in the region 14q24.3: identification of six novel transcriptsA F Roux, J M Rommens, L Read, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious pubertyD J Tomkins, A F Roux, J Waye, et al.
Genetic Testing|April 19, 2002
Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafnessN Pallares-Ruiz, P Blanchet, M Mondain, et al.
Clinical Pharmacology and Therapeutics|September 1, 1984
Metronidazole kinetics in patients with acute renal failure on dialysis: a cumulative studyA F Roux, E Moirot, B Delhotal, et al.
Revue De Laryngologie - Otologie - Rhinologie|March 8, 2008
[Usher type I syndrome in children: genotype/phenotype correlation and cochlear implant benefits]C Blanchet, A F Roux, C Hamel, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Journal Francais D'Ophtalmologie|March 16, 2005
[Molecular updates on Usher syndrome]A-F Roux
Methods in Enzymology|January 1, 1988
Alpha 1-acid glycoproteinP Arnaud, L Miribel, A F Roux
Cytogenetics and Cell Genetics|July 15, 2000
Genomic sequencing reveals the structure of the Kcnk6 and map3k11 genes and their close vicinity to the sipa1 gene on mouse chromosome 19A Saridaki, C Ferraz, J Demaille, et al.
Human Molecular Genetics|October 1, 1994
A heat shock gene at 14q22: mapping and expressionA F Roux, V T Nguyen, J A Squire, et al.
Human Molecular Genetics|June 1, 1993
Dinucleotide repeat polymorphism near the RP3 locus in Xp21 (DXS1110)A F Roux, C C Yuan, J M Rommens, et al.
Genomics|July 15, 1997
Physical and transcription map in the region 14q24.3: identification of six novel transcriptsA F Roux, J M Rommens, L Read, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious pubertyD J Tomkins, A F Roux, J Waye, et al.
Genetic Testing|April 19, 2002
Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafnessN Pallares-Ruiz, P Blanchet, M Mondain, et al.
Clinical Pharmacology and Therapeutics|September 1, 1984
Metronidazole kinetics in patients with acute renal failure on dialysis: a cumulative studyA F Roux, E Moirot, B Delhotal, et al.
Revue De Laryngologie - Otologie - Rhinologie|March 8, 2008
[Usher type I syndrome in children: genotype/phenotype correlation and cochlear implant benefits]C Blanchet, A F Roux, C Hamel, et al.
Pageof 3