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M le Merrer

Showing results (91-100 of 188) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|February 5, 1999
Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasiaP Heinz-Erian, H Schmidt, M Le Merrer, et al.
American Journal of Medical Genetics|March 1, 1994
Three new cases of the Schinzel-Giedion syndrome and review of the literatureP Labrune, S Lyonnet, V Zupan, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaliesE Vilain, M Le Merrer, C Lecointre, et al.
Journal of Medical Genetics|May 1, 1991
Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre studyA Verloes, S Aymé, D Gambarelli, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndromeV El Ghouzzi, E Lajeunie, M Le Merrer, et al.
Archives Francaises De Pediatrie|February 1, 1985
[Exclusion prenatal diagnosis of chronic familial septic granulomatosis]T Pham Huu, Y Dumez, A Durand, et al.
Journal of Medical Genetics|April 1, 1992
The orocraniodigital syndrome of Juberg and HaywardA Verloes, M Le Merrer, J C Davin, et al.
Journal of Medical Genetics|January 16, 1998
Genetic heterogeneity of Meckel syndromeJ Roume, H W Ma, M Le Merrer, et al.
Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.
Hormone Research|November 29, 2008
Pamidronate treatment of children with moderate-to-severe osteogenesis imperfecta: a note of cautionM Alharbi, G Pinto, G Finidori, et al.
Pageof 19

Showing results (91-100 of 188) with videos related to

Sort By:
Pageof 19
Journal of Pediatric Gastroenterology and Nutrition|February 5, 1999
Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasiaP Heinz-Erian, H Schmidt, M Le Merrer, et al.
American Journal of Medical Genetics|March 1, 1994
Three new cases of the Schinzel-Giedion syndrome and review of the literatureP Labrune, S Lyonnet, V Zupan, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaliesE Vilain, M Le Merrer, C Lecointre, et al.
Journal of Medical Genetics|May 1, 1991
Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre studyA Verloes, S Aymé, D Gambarelli, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndromeV El Ghouzzi, E Lajeunie, M Le Merrer, et al.
Archives Francaises De Pediatrie|February 1, 1985
[Exclusion prenatal diagnosis of chronic familial septic granulomatosis]T Pham Huu, Y Dumez, A Durand, et al.
Journal of Medical Genetics|April 1, 1992
The orocraniodigital syndrome of Juberg and HaywardA Verloes, M Le Merrer, J C Davin, et al.
Journal of Medical Genetics|January 16, 1998
Genetic heterogeneity of Meckel syndromeJ Roume, H W Ma, M Le Merrer, et al.
Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.
Hormone Research|November 29, 2008
Pamidronate treatment of children with moderate-to-severe osteogenesis imperfecta: a note of cautionM Alharbi, G Pinto, G Finidori, et al.
Pageof 19