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S Lyonnet

Showing results (111-120 of 223) with videos related to

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American Journal of Medical Genetics|May 22, 1995
Craniosynostosis and kidney malformation in a case of Hennekam syndromeV Cormier-Daire, S Lyonnet, A Lehnert, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1996
[Pregnancy and the child of a mother with phenylketonuria]V Abadie, E Depondt, J P Farriaux, et al.
Clinical Genetics|October 12, 1999
Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvementC Picard, S Couderc, T Skojaei, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
Human Genetics|February 1, 1993
A missense mutation, S349P, completely inactivates phenylalanine hydroxylase in north African Jews with phenylketonuriaM Weinstein, R C Eisensmith, V Abadie, et al.
Neurology|March 27, 2002
Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutationC Goizet, B Catargi, F Tison, et al.
The Journal of Pediatrics|June 1, 1997
Occurrence of myeloproliferative disorder in patients with Noonan syndromeB Bader-Meunier, G Tchernia, F Miélot, et al.
Human Molecular Genetics|August 13, 1998
Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung diseaseB Doray, R Salomon, J Amiel, et al.
The Journal of Pediatrics|October 13, 2001
Pierre Robin sequence: a series of 117 consecutive casesM Holder-Espinasse, V Abadie, V Cormier-Daire, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2000
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locusS Bolk, A Pelet, R M Hofstra, et al.
Pageof 23

Showing results (111-120 of 223) with videos related to

Sort By:
Pageof 23
American Journal of Medical Genetics|May 22, 1995
Craniosynostosis and kidney malformation in a case of Hennekam syndromeV Cormier-Daire, S Lyonnet, A Lehnert, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1996
[Pregnancy and the child of a mother with phenylketonuria]V Abadie, E Depondt, J P Farriaux, et al.
Clinical Genetics|October 12, 1999
Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvementC Picard, S Couderc, T Skojaei, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
Human Genetics|February 1, 1993
A missense mutation, S349P, completely inactivates phenylalanine hydroxylase in north African Jews with phenylketonuriaM Weinstein, R C Eisensmith, V Abadie, et al.
Neurology|March 27, 2002
Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutationC Goizet, B Catargi, F Tison, et al.
The Journal of Pediatrics|June 1, 1997
Occurrence of myeloproliferative disorder in patients with Noonan syndromeB Bader-Meunier, G Tchernia, F Miélot, et al.
Human Molecular Genetics|August 13, 1998
Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung diseaseB Doray, R Salomon, J Amiel, et al.
The Journal of Pediatrics|October 13, 2001
Pierre Robin sequence: a series of 117 consecutive casesM Holder-Espinasse, V Abadie, V Cormier-Daire, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2000
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locusS Bolk, A Pelet, R M Hofstra, et al.
Pageof 23