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Jacqueline Levilliers

Showing results (1-10 of 5) with videos related to

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Medecine Sciences : M/S|April 7, 2004
[Hereditary deafness: molecular genetics]Jean-Pierre Hardelin, Françoise Denoyelle, Jacqueline Levilliers, et al.
Plos Genetics|October 24, 2006
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2Catherine Dodé, Luis Teixeira, Jacqueline Levilliers, et al.
Plos One|June 14, 2014
Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafnessZied Riahi, Crystel Bonnet, Rim Zainine, et al.
Nature Genetics|March 11, 2003
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndromeCatherine Dodé, Jacqueline Levilliers, Jean-Michel Dupont, et al.
Orphanet Journal of Rare Diseases|May 17, 2011
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosisCrystel Bonnet, M'hamed Grati, Sandrine Marlin, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Medecine Sciences : M/S|April 7, 2004
[Hereditary deafness: molecular genetics]Jean-Pierre Hardelin, Françoise Denoyelle, Jacqueline Levilliers, et al.
Plos Genetics|October 24, 2006
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2Catherine Dodé, Luis Teixeira, Jacqueline Levilliers, et al.
Plos One|June 14, 2014
Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafnessZied Riahi, Crystel Bonnet, Rim Zainine, et al.
Nature Genetics|March 11, 2003
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndromeCatherine Dodé, Jacqueline Levilliers, Jean-Michel Dupont, et al.
Orphanet Journal of Rare Diseases|May 17, 2011
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosisCrystel Bonnet, M'hamed Grati, Sandrine Marlin, et al.
Pageof 1