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M le Merrer

Showing results (11-20 of 188) with videos related to

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Annales De Pediatrie|November 1, 1983
[Familial acrocephalosyndactylia]M Le Merrer, P Maroteaux, J Frézal
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 Merrer
Journal of Medical Genetics|July 1, 1991
GenochondromatosisM Le Merrer, P Fressinger, P Maroteaux
The Journal of Bone and Joint Surgery. British Volume|September 1, 1991
Pachydysostosis of the fibulaP Maroteaux, P Freisinger, M Le Merrer
Journal of Medical Genetics|March 1, 1991
Dwarfism with gloomy face: a new syndrome with features of 3-M syndromeM Le Merrer, R Brauner, P Maroteaux
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 Kallab
American Journal of Medical Genetics|November 1, 1989
BBBG syndrome or Opitz syndrome: new familyA Verloes, M Le Merrer, M L Briard
Archives Francaises De Pediatrie|January 1, 1984
[Ectodermal dysplasia and familial ectrodactyly]F Predine-Hug, M Le Merrer, J Frézal
Clinical 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 Merrer
Genetic 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 Briard
Pageof 19

Showing results (11-20 of 188) with videos related to

Sort By:
Pageof 19
Annales De Pediatrie|November 1, 1983
[Familial acrocephalosyndactylia]M Le Merrer, P Maroteaux, J Frézal
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 Merrer
Journal of Medical Genetics|July 1, 1991
GenochondromatosisM Le Merrer, P Fressinger, P Maroteaux
The Journal of Bone and Joint Surgery. British Volume|September 1, 1991
Pachydysostosis of the fibulaP Maroteaux, P Freisinger, M Le Merrer
Journal of Medical Genetics|March 1, 1991
Dwarfism with gloomy face: a new syndrome with features of 3-M syndromeM Le Merrer, R Brauner, P Maroteaux
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 Kallab
American Journal of Medical Genetics|November 1, 1989
BBBG syndrome or Opitz syndrome: new familyA Verloes, M Le Merrer, M L Briard
Archives Francaises De Pediatrie|January 1, 1984
[Ectodermal dysplasia and familial ectrodactyly]F Predine-Hug, M Le Merrer, J Frézal
Clinical 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 Merrer
Genetic 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 Briard
Pageof 19