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Clinical Genetics
|
May 1, 1994
Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects
R Newton, P Stanier, S Loughna, et al.
Current Protocols in Human Genetics
|
April 23, 2008
The Catalogue of Somatic Mutations in Cancer (COSMIC)
S A Forbes, G Bhamra, S Bamford, et al.
Genomics
|
January 1, 1996
Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3
S A Forbes, L Brennan, M Richardson, et al.
Clinical Endocrinology
|
April 18, 2003
Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism
A A J Pannett, A M Kennedy, J J O Turner, et al.
American Journal of Human Genetics
|
April 16, 1998
Characterization of mutations in patients with multiple endocrine neoplasia type 1
J H Bassett, S A Forbes, A A Pannett, et al.
Genomics
|
November 1, 1996
Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1)
A Courseaux, J Grosgeorge, P Gaudray, et al.
Human Genetics
|
September 1, 1997
Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)
S A Forbes, A A Pannett, J H Bassett, et al.
Current Protocols in Human Genetics
|
October 12, 2016
COSMIC: High-Resolution Cancer Genetics Using the Catalogue of Somatic Mutations in Cancer
S A Forbes, D Beare, N Bindal, et al.
Genomics
|
July 8, 1998
A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1
J W Höppener, M J De Wit, A Y Simarro-Doorten, et al.
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of 2
Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Clinical Genetics
|
May 1, 1994
Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects
R Newton, P Stanier, S Loughna, et al.
Current Protocols in Human Genetics
|
April 23, 2008
The Catalogue of Somatic Mutations in Cancer (COSMIC)
S A Forbes, G Bhamra, S Bamford, et al.
Genomics
|
January 1, 1996
Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3
S A Forbes, L Brennan, M Richardson, et al.
Clinical Endocrinology
|
April 18, 2003
Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism
A A J Pannett, A M Kennedy, J J O Turner, et al.
American Journal of Human Genetics
|
April 16, 1998
Characterization of mutations in patients with multiple endocrine neoplasia type 1
J H Bassett, S A Forbes, A A Pannett, et al.
Genomics
|
November 1, 1996
Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1)
A Courseaux, J Grosgeorge, P Gaudray, et al.
Human Genetics
|
September 1, 1997
Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)
S A Forbes, A A Pannett, J H Bassett, et al.
Current Protocols in Human Genetics
|
October 12, 2016
COSMIC: High-Resolution Cancer Genetics Using the Catalogue of Somatic Mutations in Cancer
S A Forbes, D Beare, N Bindal, et al.
Genomics
|
July 8, 1998
A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1
J W Höppener, M J De Wit, A Y Simarro-Doorten, et al.
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