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G Viot

Showing results (31-40 of 49) with videos related to

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The British Journal of Dermatology|March 13, 2010
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia casesN Chassaing, C Cluzeau, E Bal, et al.
L'Encephale|June 16, 2001
[French validation of a Minor Morphologic Anomalies Scale in schizophrenic patients and their parents]D Gourion, G Viot, C Goldberger, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndromeV Cormier-Daire, V Belin, V Cusin, et al.
American Journal of Medical Genetics. Part A|July 22, 2004
Atypical findings in Kabuki syndrome: report of 8 patients in a series of 20 and review of the literatureD Geneviève, J Amiel, G Viot, et al.
Nature Genetics|May 20, 1998
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)V Belin, V Cusin, G Viot, et al.
Clinical Genetics|July 3, 1998
Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndromeG Viot-Szoboszlai, J Amiel, F Doz, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 7, 2011
Prenatal diagnosis of a cleft of the tongue, lower lip and mandibleA Vincent-Rohfritsch, O Anselem, G Grangé, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Journal of Medical Genetics|March 10, 2001
A new case of exomphalos, short limbs, and macrogonadism syndromeG Viot, E Pannier, L Faivre, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
The British Journal of Dermatology|March 13, 2010
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia casesN Chassaing, C Cluzeau, E Bal, et al.
L'Encephale|June 16, 2001
[French validation of a Minor Morphologic Anomalies Scale in schizophrenic patients and their parents]D Gourion, G Viot, C Goldberger, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndromeV Cormier-Daire, V Belin, V Cusin, et al.
American Journal of Medical Genetics. Part A|July 22, 2004
Atypical findings in Kabuki syndrome: report of 8 patients in a series of 20 and review of the literatureD Geneviève, J Amiel, G Viot, et al.
Nature Genetics|May 20, 1998
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)V Belin, V Cusin, G Viot, et al.
Clinical Genetics|July 3, 1998
Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndromeG Viot-Szoboszlai, J Amiel, F Doz, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 7, 2011
Prenatal diagnosis of a cleft of the tongue, lower lip and mandibleA Vincent-Rohfritsch, O Anselem, G Grangé, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Journal of Medical Genetics|March 10, 2001
A new case of exomphalos, short limbs, and macrogonadism syndromeG Viot, E Pannier, L Faivre, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Pageof 5