Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.
about
Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transportGenetic & epigenetic approach to human obesityCohen syndrome: essential features, natural history, and heterogeneityCohen syndrome: evaluation of its cardiac, endocrine and radiological features.Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.The human obesity gene map: the 2000 update.Paternally derived translocation t(8;18)(q22.1;q22)pat associated in a patient with developmental delay: Case report and reviewThe human obesity gene map: the 2001 update.Genetics of population isolates.Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.Microsatellite marker content mapping of 12 candidate genes for obesity: assembly of seven obesity screening panels for automated genotyping.The human obesity gene map: the 2002 update.Cohen syndrome - a rare genetic cause of hypotonia in children.Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome.The ophthalmic findings in Cohen syndrome.Messages from an isolate: lessons from the Finnish gene pool.Craniofacial features in Cohen syndrome: an anthropometric and cephalometric analysis of 14 patients.Cohen syndrome with acanthosis nigricans and insulin resistance.Periodontal findings in Cohen syndrome with chronic neutropenia.Cohen syndrome in the Ohio Amish.The Human Obesity Gene Map: The 2004 Update
P2860
Q24532051-C56181F1-5092-4A1B-8A10-E918F932B0C1Q28084624-D0122661-8DEF-487F-A39E-3A150EAFCED5Q28209621-038B9605-2E9E-4DDF-B954-C4A228810E6EQ33722179-6D1B87B7-ABDE-41AF-BD9E-7EC4DF88C742Q33909933-EAAF050D-1612-4E43-A02F-326C999321FCQ34227908-1E932324-BE91-47B7-8F87-DAD405DCE295Q34244428-C6A03898-E01E-4CE1-9122-13FD4CBB82C3Q34557274-F058F6E6-9452-45A5-8F21-5B0DE92E18C8Q34657331-DB4CE598-0685-4045-B53C-6A80D2C41CACQ34754002-49FEC92A-47D3-4886-8580-DE81D538A707Q35023535-41AF8C28-CFEF-4D7A-9E39-B5F53354CD77Q35084465-F447D144-94B4-4B65-95B5-F800D5884CAFQ35146956-F183215E-3054-4654-A4A7-562EAD62056FQ35441922-617FF514-C008-4F70-9259-F25D25821F84Q35590253-250344D7-6A02-4753-ABF4-39D62A743C37Q41386249-B2561F24-AAB9-4AD6-B196-703A20E30F7AQ41922661-E697DFE7-D6A8-4FB8-B02E-779E0ABA8DB7Q41923543-2C29BB86-37AE-4790-B0B4-0B9B18E7DC24Q50951794-21033916-4CD7-4EAE-8E25-A4EA014F406DQ51939770-2F324AE5-5E2B-4770-9BC0-C7923DA4D354Q57316399-8FC3E573-AF36-4BA4-B80F-6604CCA14B05
P2860
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.
@en
type
label
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.
@en
prefLabel
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.
@en
P2093
P356
P1433
P1476
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.
@en
P2093
Sistonen P
Tahvanainen E
Weissenbach J
de la Chapelle A
P2888
P304
P356
10.1038/NG0694-201
P407
P577
1994-06-01T00:00:00Z
P6179
1043593502