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European Journal of Medical Genetics|June 10, 2006
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate regionM Chaabouni, M Le Merrer, O Raoul, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 27, 2009
Prenatal diagnosis of brachytelephalangic chondrodysplasia punctata: case reportA Benaicha, M Dommergues, J M Jouannic, et al.
Annales De Pediatrie|January 1, 1991
[A case of intrauterine dwarfism with enlargement of the cortex of the long bones]F Dusol, C Spyckerelle, F Michaux, et al.
Archives Francaises De Pediatrie|March 1, 1978
[Mucolipidosis type I. Sialidosis due to alpha-2-6-neuraminidase deficiency with neurological symptoms]P Maroteaux, M Poissonnier, M Tondeur, et al.
Journal of Medical Genetics|July 1, 1992
Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndromeJ Bonaventure, C Lasselin, J Mellier, et al.
Annales De Pediatrie|January 1, 1991
[Apert's syndrome with polymetatarsia]A Nivelon, J L Nivelon, M Matthieu, et al.
Archives Francaises De Pediatrie|October 1, 1978
[A new type of sialidosis with kidney disease: nephrosialidosis. I. Clinical, radiological and nosological study]P Maroteaux, R Humbel, G Strecker, et al.
Prenatal Diagnosis|January 24, 2007
Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic imagesM Sinico, J M Levaillant, A Vergnaud, et al.
Connective Tissue Research|January 1, 1982
The rate of collagen maturation in rat and human skinM Le Lous, J C Allain, L Cohen-Solal, et al.
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