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Audiology & Neuro-Otology
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March 18, 2010
GJB2 mutations and genotype-phenotype correlation in 335 patients from germany with nonsyndromic sensorineural hearing loss: evidence for additional recessive mutations not detected by current methods
O Bartsch, A Vatter, U Zechner, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
February 1, 1997
Cytogenetics of the genus Leporinus (Pisces, Anostomidae). 1. Karyotype analysis, heterochromatin distribution and sex chromosomes
M R Koehler, D Dehm, M Guttenbach, et al.
Genomics
|
April 16, 1998
Identification of a novel Ran binding protein 2 related gene (RANBP2L1) and detection of a gene cluster on human chromosome 2q11-q12
H G Nothwang, C Rensing, M Kübler, et al.
Cytogenetic and Genome Research
|
August 6, 2003
Chromosome banding in Amphibia. XXVI. Coexistence of homomorphic XY sex chromosomes and a derived Y-autosome translocation in Eleutherodactylus maussi (Anura, Leptodactylidae)
M Schmid, W Feichtinger, C Steinlein, et al.
Cytogenetic and Genome Research
|
December 28, 2007
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis
O Bartsch, Z Vlcková, F Erdogan, et al.
Molecular Syndromology
|
January 18, 2013
Novel VANGL1 Gene Mutations in 144 Slovakian, Romanian and German Patients with Neural Tube Defects
O Bartsch, I Kirmes, A Thiede, et al.
Genomics
|
January 8, 1999
Characterization of the mouse Src homology 3 domain gene Sh3d2c on Chr 7 demonstrates coexpression with huntingtin in the brain and identifies the processed pseudogene Sh3d2c-ps1 on Chr 2
U Zechner, S Scheel, M Hemberger, et al.
Cytogenetic and Genome Research
|
January 21, 2012
A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate cortices
E Schneider, L R Jensen, R Farcas, et al.
Genomics
|
February 1, 1997
Construction and characterization of a 10-genome equivalent yeast artificial chromosome library for the laboratory rat, Rattus norvegicus
L Cai, L C Schalkwyk, A Schoeberlein-Stehli, et al.
Andrology
|
September 3, 2013
Broad DNA methylation changes of spermatogenesis, inflammation and immune response-related genes in a subgroup of sperm samples for assisted reproduction
B Schütte, N El Hajj, J Kuhtz, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 170) with videos related to
Sort By:
Page
of 17
Audiology & Neuro-Otology
|
March 18, 2010
GJB2 mutations and genotype-phenotype correlation in 335 patients from germany with nonsyndromic sensorineural hearing loss: evidence for additional recessive mutations not detected by current methods
O Bartsch, A Vatter, U Zechner, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
February 1, 1997
Cytogenetics of the genus Leporinus (Pisces, Anostomidae). 1. Karyotype analysis, heterochromatin distribution and sex chromosomes
M R Koehler, D Dehm, M Guttenbach, et al.
Genomics
|
April 16, 1998
Identification of a novel Ran binding protein 2 related gene (RANBP2L1) and detection of a gene cluster on human chromosome 2q11-q12
H G Nothwang, C Rensing, M Kübler, et al.
Cytogenetic and Genome Research
|
August 6, 2003
Chromosome banding in Amphibia. XXVI. Coexistence of homomorphic XY sex chromosomes and a derived Y-autosome translocation in Eleutherodactylus maussi (Anura, Leptodactylidae)
M Schmid, W Feichtinger, C Steinlein, et al.
Cytogenetic and Genome Research
|
December 28, 2007
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis
O Bartsch, Z Vlcková, F Erdogan, et al.
Molecular Syndromology
|
January 18, 2013
Novel VANGL1 Gene Mutations in 144 Slovakian, Romanian and German Patients with Neural Tube Defects
O Bartsch, I Kirmes, A Thiede, et al.
Genomics
|
January 8, 1999
Characterization of the mouse Src homology 3 domain gene Sh3d2c on Chr 7 demonstrates coexpression with huntingtin in the brain and identifies the processed pseudogene Sh3d2c-ps1 on Chr 2
U Zechner, S Scheel, M Hemberger, et al.
Cytogenetic and Genome Research
|
January 21, 2012
A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate cortices
E Schneider, L R Jensen, R Farcas, et al.
Genomics
|
February 1, 1997
Construction and characterization of a 10-genome equivalent yeast artificial chromosome library for the laboratory rat, Rattus norvegicus
L Cai, L C Schalkwyk, A Schoeberlein-Stehli, et al.
Andrology
|
September 3, 2013
Broad DNA methylation changes of spermatogenesis, inflammation and immune response-related genes in a subgroup of sperm samples for assisted reproduction
B Schütte, N El Hajj, J Kuhtz, et al.
Page
of 17