About: Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.

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About: Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. Goto Sponge NotDistinct Permalink

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scientific article published on August 1991

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rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 1991 (ast) наукова стаття, опублікована в серпні 1991 (uk) مقالة علمية نشرت في أغسطس 1991 (ar) scientific article published on August 1991 (en)
publication date	wds:Q37271892-2E5B6FA1-7C8E-4218-B57E-089D43B29697
publication date	1991-08-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q37271892-04C382E1-7A5F-44C4-99C6-E9F3AAB6B577 wds:Q37271892-0D6EC18D-4541-41BB-B42B-7604BEFB340A wds:Q37271892-0FACEB82-8F41-43CB-B8D5-3FC9FC41BB1D wds:Q37271892-2472D1B1-7647-4C5D-86C8-93934853DD0E wds:Q37271892-26BDAEA6-95AF-46DA-925B-4A247F17DDEB wds:Q37271892-38309EEA-036C-4548-869A-B397E737E5FD wds:Q37271892-57360149-71A9-469A-925B-42DE64A64186 wds:Q37271892-643E90C3-60AF-4A6B-B8A1-90FEADF77C48 wds:Q37271892-7004E404-A6EB-4CC0-8F4C-4BAB4B1A2006 wds:Q37271892-748048E8-4C7E-4549-AAD0-E7DD2E435E63 wds:Q37271892-821B627C-E4EE-45D0-B96D-733371685D63 wds:Q37271892-9A0C9C1C-82E9-4F02-95FC-BC11CEE17224 wds:Q37271892-9B2C80E4-26C3-4F63-9C36-F03575B1F7DA wds:Q37271892-9B968650-295E-40CE-998F-6D2E132CF3F3 wds:Q37271892-9EEFF33B-C452-4C75-8543-361EF8CD675C wds:Q37271892-A78BF646-CD4C-48A4-AB50-6D23685006A2 wds:Q37271892-B1109F2D-F1CF-4B22-A74A-C5EDDA241010 wds:Q37271892-BDD4A686-0533-41CB-BF33-3AAD0768100A wds:Q37271892-C407975B-530F-493F-B346-29CCEBF0190A wds:Q37271892-C4194F97-E0E8-486D-BD8B-C114ECAD188A wds:Q37271892-DE48A3EC-63CF-4D73-8FF2-322081D8AE2D wds:Q37271892-E9A3CBD9-50A0-4756-950B-37CB01700710
cites work	Interstitial deletion of the short arm of chromosome 7 without craniosynostosis Gonadal and extragonadal expression of inhibin alpha, beta A, and beta B subunits in various tissues predicts diverse functions Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13. The Greig cephalopolysyndactyly syndrome. A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome Chromosome maps of man and mouse, III. Human gamma-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7. Cognate homeo-box loci mapped on homologous human and mouse chromosomes Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities A patient with interstitial deletion 7 (p13 leads to p21) The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature The Greig polysyndactyly-craniofacial dysmorphism syndrome Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13). Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13). Familial polysyndactyly and craniofacial anomalies. Greig cephalopolysyndactyly: report of 13 affected individuals in three families. Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes) Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes Report of the committee on the genetic constitution of chromosomes 7 and 8. Chromosomal locations of the murine T-cell receptor alpha-chain gene and the T-cell gamma gene A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21. wd:Q56420438
author name string	wds:Q37271892-798FCDDE-DE8E-42B0-A2EC-C21E894EABED wds:Q37271892-CFDB1773-BFFB-4B01-9D56-AE91F0A16AFA wds:Q37271892-DE3902CD-41D3-4D88-9B6A-3671142B5360 wds:Q37271892-F84D4D72-D522-4515-8DF2-B533CBACE97A
author name string	C T Caskey D H Ledbetter F Greenberg A L Pettigrew
rdfs:label	Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (en) Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (nl) Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (ast)
skos:prefLabel	Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (en) Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (nl) Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (ast)
name	Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (en) Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (nl) Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (ast)
title	wds:Q37271892-229FCAA1-EC42-46D1-8D67-F2EF41D8744C
title	Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. (en)
page(s)	wds:Q37271892-E2193DF4-2931-45D8-81F3-0457B782D6C0
page(s)	452-456
instance of	wds:Q37271892-085A9B21-8601-4682-BE58-B52031E91ABA
instance of	scholarly article
PubMed ID	wds:Q37271892-3AD5F775-ED77-4C5C-B410-48416CA33EA2
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1879832
PubMed ID	1879832
published in	wds:Q37271892-1D656FEF-A230-4DB6-B12D-87B7346D3267
published in	Human Genetics
issue	wds:Q37271892-8F475D0C-9456-476E-A098-4CB9D12269B5
volume	wds:Q37271892-E32DEB30-0F86-4D00-900E-261303776BA9
issue	4
volume	87
DOI	wds:Q37271892-E003E9CE-E09B-4523-B565-A438F11AF113
DOI	http://dx.doi.org/10.1007/BF00197167
DOI	10.1007/BF00197167
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37271892
is cites work of	Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders

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