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American Journal of Medical Genetics. Part A|September 11, 2003
Spondyloepimetaphyseal dysplasia with multiple dislocations, leptodactylic type: report of a new patient and review of the literatureA Mégarbané, I Ghanem, M Le MerrerAmerican Journal of Medical Genetics|July 23, 1998
Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2V Cormier-Daire, A Superti-Furga, A Munnich, 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.Clinical Dysmorphology|July 1, 1997
Ptosis, down-slanting palpebral fissures, hypertelorism, seizures and mental retardation: a possible new MCA/MR syndromeA Mégarbané, M Le Merrer, K el KallabAmerican Journal of Medical Genetics|November 1, 1989
BBBG syndrome or Opitz syndrome: new familyA Verloes, M Le Merrer, M L BriardArchives Francaises De Pediatrie|January 1, 1984
[Ectodermal dysplasia and familial ectrodactyly]F Predine-Hug, M Le Merrer, J FrézalClinical Genetics|January 24, 1998
Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndromeG Plessis, M Le Treust, M Le MerrerGenetic Counseling (Geneva, Switzerland)|January 1, 1991
Scalp defect, nipples absence and ears abnormalities: an other case of Finlay syndromeM Le Merrer, D Renier, M L BriardArchives Francaises De Pediatrie|March 1, 1980
[Osteomesopycnosis. A new autosomal dominant osteosclerosing bone disease (author's transl)]P MaroteauxHuman Genetics|May 1, 1989
Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive formP MaroteauxPageof 29