About: Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome

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About: Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 1985

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1985 (uk) im Jahr 1985 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 1985 (ast) artikull shkencor i botuar më 01 janar 1985 (sq) scientific article published on 01 January 1985 (en)
publication date	wds:Q70060114-32946DAD-AE4C-4170-8B80-C057EA40DFEB
publication date	1985-01-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q70060114-8866850B-03E4-4047-B1F5-A573571C55F7
exact match	https://scigraph.springernature.com/pub.10.1007/bf00293277
cites work	wds:Q70060114-09114D86-B23D-44DA-846D-EE76F266D60F wds:Q70060114-1957F1D0-9B81-43FF-B36E-F1FC5EE2B9CF wds:Q70060114-55C1BCC9-CA0B-43C7-A2A9-45F365BC1C32 wds:Q70060114-56FD3753-0614-4317-A67A-D744055CE76A wds:Q70060114-71002E9F-A073-433F-9747-6A1127C6053B wds:Q70060114-A1F58189-3996-4145-9290-45A792964BA9 wds:Q70060114-AEFA7A64-922D-4E06-A673-D05B3DCA33FA wds:Q70060114-BE1780CA-56D8-476B-95FF-35EBD9F2B841 wds:Q70060114-C0AA2277-D00F-481B-9C11-588FED3BB97C wds:Q70060114-CB3B2767-4EF6-40C0-92BF-357F24869557 wds:Q70060114-EE93F2BF-D52F-4D2A-9338-54E74FB0884B wds:Q70060114-FC22A940-A67F-4CAE-8433-58B690E1D98A
cites work	Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X. A marker X chromosome On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression The fragile X syndrome: the patients and their chromosomes Activity of the fragile X in heterozygous carriers Brief report: linkage between G6PD and fragile-X syndrome Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male Replication status of the fragile X chromosome, fra(X)(q27), in three heterozygous females. Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q). Expression of the fragile site Xq27 in fibroblasts. I. Detection of fra(X)(q27) in fibroblast clones from males with X-linked mental retardation. Expression of the fragile site Xq27 in fibroblasts. II. Evidence for negative and positive clones from heterozygous females and possible relationship between frequency and phenotype. Manifestation of the fragile site Xq27 in fibroblasts. III. A method to demonstrate R-type replication patterns and the fragile site
author name string	wds:Q70060114-22433DA8-69C1-416C-9292-7223230773D3 wds:Q70060114-24F6BC3B-9622-45C2-B725-A5777E314AE3 wds:Q70060114-30F8DB7F-C1EB-421E-960F-0F55BACC667C wds:Q70060114-79D7002C-E8E5-4984-8177-51C31578B7B6
author name string	W Vogel G Barbi P Steinbach S Baur
rdfs:label	Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (en) Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (nl) Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (sq)
skos:prefLabel	Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (en) Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (nl) Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (sq)
name	Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (en) Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (nl) Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (sq)
title	wds:Q70060114-8E19F853-10C9-44AF-9DDE-E0BAAA07FD05
title	Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome (en)
page(s)	wds:Q70060114-AE736E45-C6D2-4368-B37C-6A9B74DCDDC6
page(s)	106-108
instance of	wds:Q70060114-42AD64C7-6C17-4C89-B631-78970490C9D8
instance of	scholarly article
main subject	wds:Q70060114-1C4F1016-157D-488A-B82C-1493130B644B
main subject	heterozygosity
PubMed ID	wds:Q70060114-45F58F6F-C521-4352-851F-0457FEC9F144
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3972411
PubMed ID	3972411
published in	wds:Q70060114-52A8B8B2-F333-4D77-AA68-381146871E69
published in	Human Genetics
issue	wds:Q70060114-D2C13D11-4B4E-45F5-84B4-8A817700970D
volume	wds:Q70060114-111F3546-5A66-4423-BBF4-655BDFD312ED
issue	2
volume	69
DOI	wds:Q70060114-BC413BB2-8134-4657-8CB2-AB5D2CE757C7
DOI	http://dx.doi.org/10.1007/BF00293277
DOI	10.1007/BF00293277
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70060114
is cites work of	Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome. Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologue Fragile X syndrome: clinical, cytogenetic, biochemical and molecular features
is cites work of	wds:Q68583884-7A1095BB-7D4F-4006-ACF8-1618F77948AD wds:Q52079380-04908069-C22A-4113-9F08-9A4BCE08DCB5 wds:Q69723327-38774889-2611-4AA3-BE82-D38CA9DF6996

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