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A Moncla

Showing results (11-20 of 51) with videos related to

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Clinical Dysmorphology|November 21, 1998
Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2S Sigaudy, A Moncla, C Fredouille, et al.
Hormone Research|January 9, 2001
Auxological and endocrine evolution of 28 children with Prader-Willi syndrome: effect of GH therapy in 14 childrenM Tauber, C Barbeau, B Jouret, et al.
Annales De Genetique|January 1, 1989
[Diagnosis of minor chromosome modifications by molecular cytogenetics]S Taviaux, A Moncla, F Giraud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 16, 1998
[Smith-Magenis syndrome]M O Livet, A Moncla, B Delobel, et al.
Clinical Dysmorphology|October 1, 1995
Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndromeN Philip, L Andrac, A Moncla, et al.
American Journal of Medical Genetics|July 24, 1998
Atypical molecular findings identify limits of technical screening tests for Prader-Willi and Angelman syndrome diagnosesP Malzac, A Moncla, K Pedeillier, et al.
American Journal of Medical Genetics|November 4, 1998
Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literatureS Sigaudy, A Toutain, A Moncla, et al.
Journal of Medical Genetics|September 1, 1991
Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new casesA Moncla, M O Livet, M Auger, et al.
Journal of Medical Genetics|December 1, 1998
Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication studyC Stavropoulou, C Mignon, B Delobel, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effectC Mignon, P Malzac, A Moncla, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Clinical Dysmorphology|November 21, 1998
Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2S Sigaudy, A Moncla, C Fredouille, et al.
Hormone Research|January 9, 2001
Auxological and endocrine evolution of 28 children with Prader-Willi syndrome: effect of GH therapy in 14 childrenM Tauber, C Barbeau, B Jouret, et al.
Annales De Genetique|January 1, 1989
[Diagnosis of minor chromosome modifications by molecular cytogenetics]S Taviaux, A Moncla, F Giraud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 16, 1998
[Smith-Magenis syndrome]M O Livet, A Moncla, B Delobel, et al.
Clinical Dysmorphology|October 1, 1995
Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndromeN Philip, L Andrac, A Moncla, et al.
American Journal of Medical Genetics|July 24, 1998
Atypical molecular findings identify limits of technical screening tests for Prader-Willi and Angelman syndrome diagnosesP Malzac, A Moncla, K Pedeillier, et al.
American Journal of Medical Genetics|November 4, 1998
Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literatureS Sigaudy, A Toutain, A Moncla, et al.
Journal of Medical Genetics|September 1, 1991
Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new casesA Moncla, M O Livet, M Auger, et al.
Journal of Medical Genetics|December 1, 1998
Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication studyC Stavropoulou, C Mignon, B Delobel, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effectC Mignon, P Malzac, A Moncla, et al.
Pageof 6