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M le Merrer

Showing results (151-160 of 188) with videos related to

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American Journal of Medical Genetics|October 12, 2002
Clinical and genetic heterogeneity of Seckel syndromeL Faivre, M Le Merrer, S Lyonnet, et al.
American Journal of Medical Genetics|December 5, 2000
Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndromeL Faivre, A M Prieur, M Le Merrer, et al.
Nature Genetics|January 1, 1997
Mutations of the TWIST gene in the Saethre-Chotzen syndromeV el Ghouzzi, M Le Merrer, F Perrin-Schmitt, et al.
Journal of Medical Genetics|April 5, 2003
Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3L Faivre, M Le Merrer, L I Al-Gazali, et al.
Journal of Medical Genetics|March 2, 1999
A new lethal syndrome of exomphalos, short limbs, and macrogonadismL Faivre, A L Delezoide, F Narcy, et al.
Journal of Medical Genetics|March 8, 2003
Clinical, radiological, and chondro-osseous findings in opsismodysplasia: survey of a series of 12 unreported casesV Cormier-Daire, A L Delezoide, N Philip, et al.
Journal of Medical Genetics|October 4, 2002
Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1C Thauvin-Robinet, V El Ghouzzi, W Chemaitilly, et al.
Annales De Genetique|January 1, 1985
Embryonic testicular regression syndrome and severe mental retardation in sibsJ de Grouchy, A Gompel, Y Salomon-Bernard, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 5, 2012
Three-dimensional helical computed tomography in prenatal diagnosis of fetal skeletal dysplasiaG Macé, P Sonigo, V Cormier-Daire, et al.
Human Genetics|January 5, 2007
A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34B Isidor, N Dagoneau, C Huber, et al.
Pageof 19

Showing results (151-160 of 188) with videos related to

Sort By:
Pageof 19
American Journal of Medical Genetics|October 12, 2002
Clinical and genetic heterogeneity of Seckel syndromeL Faivre, M Le Merrer, S Lyonnet, et al.
American Journal of Medical Genetics|December 5, 2000
Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndromeL Faivre, A M Prieur, M Le Merrer, et al.
Nature Genetics|January 1, 1997
Mutations of the TWIST gene in the Saethre-Chotzen syndromeV el Ghouzzi, M Le Merrer, F Perrin-Schmitt, et al.
Journal of Medical Genetics|April 5, 2003
Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3L Faivre, M Le Merrer, L I Al-Gazali, et al.
Journal of Medical Genetics|March 2, 1999
A new lethal syndrome of exomphalos, short limbs, and macrogonadismL Faivre, A L Delezoide, F Narcy, et al.
Journal of Medical Genetics|March 8, 2003
Clinical, radiological, and chondro-osseous findings in opsismodysplasia: survey of a series of 12 unreported casesV Cormier-Daire, A L Delezoide, N Philip, et al.
Journal of Medical Genetics|October 4, 2002
Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1C Thauvin-Robinet, V El Ghouzzi, W Chemaitilly, et al.
Annales De Genetique|January 1, 1985
Embryonic testicular regression syndrome and severe mental retardation in sibsJ de Grouchy, A Gompel, Y Salomon-Bernard, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 5, 2012
Three-dimensional helical computed tomography in prenatal diagnosis of fetal skeletal dysplasiaG Macé, P Sonigo, V Cormier-Daire, et al.
Human Genetics|January 5, 2007
A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34B Isidor, N Dagoneau, C Huber, et al.
Pageof 19