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C Braun-Quentin

Showing results (1-10 of 8) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Genetic nosology and counseling of humeroradial synostosisR A Pfeiffer, C Braun-Quentin
Clinical Genetics|August 1, 1996
De novo direct duplication 3 (p25-->pter): a previously undescribed chromosomal aberrationD Kotzot, C Krüger, C Braun-Quentin
American Journal of Medical Genetics|September 6, 1996
Variant of Coffin-Siris syndrome or previously undescribed syndrome?C Braun-Quentin, L Kapferer, D Kotzot
Journal of Medical Genetics|July 1, 1996
MURCS association: case report and reviewC Braun-Quentin, C Billes, B Böwing, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
RNA-based mutation screening in German families with Sjögren-Larsson syndromeC Kraus, C Braun-Quentin, W G Ballhausen, et al.
Acta Dermato-Venereologica|March 23, 1999
Further evidence of genetic homogeneity in Sjögren-Larsson syndromeM Pigg, I Annton-Lamprecht, C Braun-Quentin, et al.
Human Mutation|November 26, 1998
Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndromeA Sillén, I Anton-Lamprecht, C Braun-Quentin, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Isochromosome 18p results from maternal meiosis II nondisjunctionD Kotzot, G Bundscherer, F Bernasconi, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Genetic nosology and counseling of humeroradial synostosisR A Pfeiffer, C Braun-Quentin
Clinical Genetics|August 1, 1996
De novo direct duplication 3 (p25-->pter): a previously undescribed chromosomal aberrationD Kotzot, C Krüger, C Braun-Quentin
American Journal of Medical Genetics|September 6, 1996
Variant of Coffin-Siris syndrome or previously undescribed syndrome?C Braun-Quentin, L Kapferer, D Kotzot
Journal of Medical Genetics|July 1, 1996
MURCS association: case report and reviewC Braun-Quentin, C Billes, B Böwing, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
RNA-based mutation screening in German families with Sjögren-Larsson syndromeC Kraus, C Braun-Quentin, W G Ballhausen, et al.
Acta Dermato-Venereologica|March 23, 1999
Further evidence of genetic homogeneity in Sjögren-Larsson syndromeM Pigg, I Annton-Lamprecht, C Braun-Quentin, et al.
Human Mutation|November 26, 1998
Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndromeA Sillén, I Anton-Lamprecht, C Braun-Quentin, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Isochromosome 18p results from maternal meiosis II nondisjunctionD Kotzot, G Bundscherer, F Bernasconi, et al.
Pageof 1