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Human Genetics
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October 28, 1997
A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region
O Bartsch, G K Hinkel, M B Petersen, et al.
Human Genetics
|
November 1, 1995
DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor
S Schuffenhauer, O Bartsch, M Stumm, et al.
Molecular Syndromology
|
February 20, 2014
Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss
B Vona, C Neuner, N El Hajj, et al.
American Journal of Human Genetics
|
April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11
O Bartsch, W Wuyts, W Van Hul, et al.
Clinical Genetics
|
March 13, 2016
Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis
S Boppudi, N Bögershausen, H B Hove, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 65) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 65 results.
Human Genetics
|
October 28, 1997
A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region
O Bartsch, G K Hinkel, M B Petersen, et al.
Human Genetics
|
November 1, 1995
DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor
S Schuffenhauer, O Bartsch, M Stumm, et al.
Molecular Syndromology
|
February 20, 2014
Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss
B Vona, C Neuner, N El Hajj, et al.
American Journal of Human Genetics
|
April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11
O Bartsch, W Wuyts, W Van Hul, et al.
Clinical Genetics
|
March 13, 2016
Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis
S Boppudi, N Bögershausen, H B Hove, et al.
Page
of 7