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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.European Journal of Pediatrics|May 1, 1980
The mild form of pseudoachondroplasia. Identity of the morphological and biochemical alterations of growth cartilage with those of typical pseudoachondroplasiaP Maroteaux, R Stanescu, V Stanescu, et al.European Journal of Pediatrics|May 1, 1988
Recessive lethal chondrodysplasia, "round femoral inferior epiphysis type"P Maroteaux, R Stanescu, V Stanescu, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1996
[Odontochondrodysplasia]P Maroteaux, V Briscioli, F Lalatta, et al.The Journal of Bone and Joint Surgery. American Volume|October 1, 1990
Spondyloepiphyseal dysplasia of MaroteauxA N Doman, P Maroteaux, E D LyneAnnales De Genetique|January 1, 1988
Comparative histopathology of the growth cartilage in short-rib polydactyly syndromes type I and type III and in chondroectodermal dysplasiaM Erzen, R Stanescu, V Stanescu, 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.Radiology|February 1, 1975
The Dyggve-Melchior-Clausen syndromeJ Spranger, P Maroteaux, V M Der KaloustianPageof 29