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Genetic Counseling (Geneva, Switzerland)
|
May 3, 2001
De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21
M Riegel, A Baumer, A Piram, et al.
Human Molecular Genetics
|
May 23, 1998
High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions
A Baumer, F Dutly, D Balmer, et al.
Human Mutation
|
January 1, 1997
Method for in situ investigation of mitochondrial DNA deletions
S A Kovalenko, P J Harms, M Tanaka, et al.
Neuroreport
|
July 8, 1996
The Gly/Glu polymorphism of the neurotrophin 3 gene: allele frequencies in a Caucasian population and relevance for psychiatric disorders
J Thome, A Baumer, A Harsányi, et al.
Human Mutation
|
June 30, 2000
Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS
N Blau, T Scherer-Oppliger, A Baumer, et al.
Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer
|
January 1, 1997
Exploring the role of oxygen in Fanconi's anemia
W Liebetrau, T M Rünge, A Baumer, et al.
Clinical Genetics
|
April 25, 2006
Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene
D Bartholdi, A Klein, M Weissert, et al.
European Journal of Human Genetics : EJHG
|
December 31, 1997
Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy
A Schinzel, D Kotzot, L Brecevic, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 2, 2005
M-FISH applications in clinical genetics
Z Cetin, S Berker Karaüzüm, S Yakut, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 27, 2010
A homoallelic FECH mutation in a patient with both erythropoietic protoporphyria and palmar keratoderma
E I Minder, X Schneider-Yin, R Mamet, et al.
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of 7
Search research articles
Search
Showing results (41-50 of 63) with videos related to
Sort By:
Page
of 7
Genetic Counseling (Geneva, Switzerland)
|
May 3, 2001
De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21
M Riegel, A Baumer, A Piram, et al.
Human Molecular Genetics
|
May 23, 1998
High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions
A Baumer, F Dutly, D Balmer, et al.
Human Mutation
|
January 1, 1997
Method for in situ investigation of mitochondrial DNA deletions
S A Kovalenko, P J Harms, M Tanaka, et al.
Neuroreport
|
July 8, 1996
The Gly/Glu polymorphism of the neurotrophin 3 gene: allele frequencies in a Caucasian population and relevance for psychiatric disorders
J Thome, A Baumer, A Harsányi, et al.
Human Mutation
|
June 30, 2000
Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS
N Blau, T Scherer-Oppliger, A Baumer, et al.
Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer
|
January 1, 1997
Exploring the role of oxygen in Fanconi's anemia
W Liebetrau, T M Rünge, A Baumer, et al.
Clinical Genetics
|
April 25, 2006
Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene
D Bartholdi, A Klein, M Weissert, et al.
European Journal of Human Genetics : EJHG
|
December 31, 1997
Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy
A Schinzel, D Kotzot, L Brecevic, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 2, 2005
M-FISH applications in clinical genetics
Z Cetin, S Berker Karaüzüm, S Yakut, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 27, 2010
A homoallelic FECH mutation in a patient with both erythropoietic protoporphyria and palmar keratoderma
E I Minder, X Schneider-Yin, R Mamet, et al.
Page
of 7