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L Faivre

Showing results (41-50 of 131) with videos related to

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European Journal of Medical Genetics|March 23, 2011
Written information to patients in clinical genetics: what's the impact?C Cassini, C Thauvin-Robinet, S Vinault, et al.
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.
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|June 3, 2004
A novel form of syndromic cutis laxa with facial dysmorphism, cleft palate, and mental retardationD Genevieve, C Baumann, C Huber, 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 the European Academy of Dermatology and Venereology : JEADV|April 30, 2021
Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutationsM Theiler, L Weibel, S Christen-Zaech, et al.
Prenatal Diagnosis|October 4, 2000
Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiencyL Faivre, V Cormier-Daire, D Chrétien, et al.
Prenatal Diagnosis|August 12, 2009
Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20P Callier, L Faivre, S Pigeonnat, et al.
Pageof 14

Showing results (41-50 of 131) with videos related to

Sort By:
Pageof 14
European Journal of Medical Genetics|March 23, 2011
Written information to patients in clinical genetics: what's the impact?C Cassini, C Thauvin-Robinet, S Vinault, et al.
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.
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|June 3, 2004
A novel form of syndromic cutis laxa with facial dysmorphism, cleft palate, and mental retardationD Genevieve, C Baumann, C Huber, 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 the European Academy of Dermatology and Venereology : JEADV|April 30, 2021
Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutationsM Theiler, L Weibel, S Christen-Zaech, et al.
Prenatal Diagnosis|October 4, 2000
Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiencyL Faivre, V Cormier-Daire, D Chrétien, et al.
Prenatal Diagnosis|August 12, 2009
Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20P Callier, L Faivre, S Pigeonnat, et al.
Pageof 14