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M Le Merrer

Showing results (81-90 of 188) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1997
[Fibroblast growth factor receptors and hereditary abnormalities of bone growth]J Bonaventure, F Rousseau, L Legeai-Mallet, et al.
Human Genetics|August 1, 1996
Possible genetic heterogeneity in the Saethre-Chotzen syndromeH W Ma, E Lajeunie, N de Parseval, et al.
The Journal of Bone and Joint Surgery. British Volume|October 13, 1998
Progressive osseous heteroplasia. Report of a familyJ A Urtizberea, H Testart, F Cartault, et al.
Journal of Medical Genetics|July 7, 2000
Genitopatellar syndrome: a new condition comprising absent patellae, scrotal hypoplasia, renal anomalies, facial dysmorphism, and mental retardationV Cormier-Daire, M L Chauvet, S Lyonnet, et al.
European Journal of Pediatrics|September 1, 2000
Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophyP Castelnau, M Le Merrer, C Diatloff-Zito, et al.
Annales De Genetique|January 1, 1984
[Association of VACTERL and hydrocephalus: a new familial entity]M L Briard, M le Merrer, H Plauchu, et al.
American Journal of Human Genetics|March 26, 1999
COL9A3: A third locus for multiple epiphyseal dysplasiaP Paassilta, J Lohiniva, S Annunen, et al.
Human Genetics|October 1, 1995
Genetic mapping of Xp22.12-p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL)S Heuertz, A Smahi, A O Wilkie, et al.
The Journal of Clinical Investigation|July 3, 1998
Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasiaA S Jobert, P Zhang, A Couvineau, et al.
Annales De Genetique|January 1, 1988
CFC syndrome: a syndrome distinct from Noonan syndromeA Verloes, M Le Merrer, D Soyeur, et al.
Pageof 19

Showing results (81-90 of 188) with videos related to

Sort By:
Pageof 19
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1997
[Fibroblast growth factor receptors and hereditary abnormalities of bone growth]J Bonaventure, F Rousseau, L Legeai-Mallet, et al.
Human Genetics|August 1, 1996
Possible genetic heterogeneity in the Saethre-Chotzen syndromeH W Ma, E Lajeunie, N de Parseval, et al.
The Journal of Bone and Joint Surgery. British Volume|October 13, 1998
Progressive osseous heteroplasia. Report of a familyJ A Urtizberea, H Testart, F Cartault, et al.
Journal of Medical Genetics|July 7, 2000
Genitopatellar syndrome: a new condition comprising absent patellae, scrotal hypoplasia, renal anomalies, facial dysmorphism, and mental retardationV Cormier-Daire, M L Chauvet, S Lyonnet, et al.
European Journal of Pediatrics|September 1, 2000
Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophyP Castelnau, M Le Merrer, C Diatloff-Zito, et al.
Annales De Genetique|January 1, 1984
[Association of VACTERL and hydrocephalus: a new familial entity]M L Briard, M le Merrer, H Plauchu, et al.
American Journal of Human Genetics|March 26, 1999
COL9A3: A third locus for multiple epiphyseal dysplasiaP Paassilta, J Lohiniva, S Annunen, et al.
Human Genetics|October 1, 1995
Genetic mapping of Xp22.12-p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL)S Heuertz, A Smahi, A O Wilkie, et al.
The Journal of Clinical Investigation|July 3, 1998
Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasiaA S Jobert, P Zhang, A Couvineau, et al.
Annales De Genetique|January 1, 1988
CFC syndrome: a syndrome distinct from Noonan syndromeA Verloes, M Le Merrer, D Soyeur, et al.
Pageof 19