About: Colour Vision Studies and the X-Chromosome Constitution of Patients with Klinefelter's Syndrome

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About: Colour Vision Studies and the X-Chromosome Constitution of Patients with Klinefelter's Syndrome Goto Sponge NotDistinct Permalink

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scientific article published in Nature

Attributes	Values
rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) article publié dans la revue scientifique Nature (fr) scientific article published in Nature (en) im Oktober 1958 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована в Nature в жовтні 1958 (uk)
publication date	wds:Q58949110-CECA6AD9-798A-49D3-AA78-7B1BDA151626
publication date	1958-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58949110-973225D6-A723-4693-9D52-D7D837D477C9
language of work or name	English
exact match	wds:Q58949110-A5FBF150-AD9D-433E-B450-7812DEC1A9AD
exact match	https://scigraph.springernature.com/pub.10.1038/1821092a0
cites work	wds:Q58949110-801CAE9A-A97D-44ED-BD41-65FB5C192D9E wds:Q58949110-ADD4A10A-6CBF-486F-A9D4-8639C6EBE2A9 wds:Q58949110-FA077389-7FB5-486C-A633-23595C62DA70 wds:Q58949110-FB6C1E7C-0F4B-44B0-B95D-BDD429A612EB
cites work	Colour-blindness in ovarian agenesis (gonadal dysplasia) A morphological distinction between neurones of the male and female, and the behaviour of the nucleolar satellite during accelerated nucleoprotein synthesis Human Somatic Chromosomes Klinefelter's syndrome; frequency and testicular morphology in relation to nuclear sex
author name string	wds:Q58949110-50604324-014D-4871-83F1-395409D7F731 wds:Q58949110-7D21773A-9FCD-4A09-976B-800D68E48475 wds:Q58949110-840300F3-947E-4C9E-8510-899DEEA4D43F wds:Q58949110-A7EFEB0B-F066-4752-8DFA-A57904C109DA wds:Q58949110-AA6E0DB2-1FCC-4F5B-90DD-FD63C432C697 wds:Q58949110-C64ECDD3-F745-4367-9239-8D1FBAA8D4F8
author name string	B LENNOX A PRADER J S STEWART M A FERGUSON-SMITH P E POLANI P M BISHOP
rdfs:label	Colour Vision Studies and the X-Chromosome Constitution of Patients with Klinefelter's Syndrome (en) Colour Vision Studies and the X-Chromosome Constitution of Patients with Klinefelter's Syndrome (nl)
skos:prefLabel	Colour Vision Studies and the X-Chromosome Constitution of Patients with Klinefelter's Syndrome (en) Colour Vision Studies and the X-Chromosome Constitution of Patients with Klinefelter's Syndrome (nl)
name	Colour Vision Studies and the X-Chromosome Constitution of Patients with Klinefelter's Syndrome (en) Colour Vision Studies and the X-Chromosome Constitution of Patients with Klinefelter's Syndrome (nl)
title	wds:Q58949110-88DBAB69-D1FA-4166-8BF6-D014EDBC62A5
title	Colour vision studies and the x-chromosome constitution of patients with Klinefelter's syndrome (en)
page(s)	wds:Q58949110-37819BAE-CE76-482B-85BE-1803E2DC82A9
page(s)	1092-1093
instance of	wds:Q58949110-E2513616-BE86-495C-B5A2-5970BB8A17A8
instance of	scholarly article
main subject	wds:Q58949110-FC1DFCF3-9362-430C-A1C2-30CF9CC1C5DE
main subject	Klinefelter's syndrome
PubMed ID	wds:Q58949110-AC0EFE64-BC41-416B-9349-5C6C61857C25
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13590234
PubMed ID	13590234
published in	wds:Q58949110-BD89721F-BE45-4BE5-8907-2C70A76610F4
published in	Nature
issue	wds:Q58949110-FC8BD730-2A07-4B84-AB38-EA118D035FBC
volume	wds:Q58949110-EE16DE1F-1ABA-4C81-9657-62B033FA84FC
issue	4642
volume	182
DOI	wds:Q58949110-B1F59A43-66EB-45E1-8679-233B8892942C
DOI	http://dx.doi.org/10.1038/1821092A0
DOI	10.1038/1821092A0
Fatcat ID	wds:Q58949110-F0C3DD29-B080-4C5F-8DF4-80A4DB3AA6B1
Fatcat ID	release_squ7ddwr5bg47oqjvhymo6uiiy
Dimensions Publication ID	wds:Q58949110-AC3D55CD-48FD-488B-8237-6CF09CB62008
Dimensions Publication ID	1029483431
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58949110
is cites work of	Growing points in cell pathology. Cytogenetic aspects A case of human intersexuality having a possible XXY sex-determining mechanism Colour-blindness in Klinefelter's Syndrome Sex Determination: Diagnostic Methods. Sex chromatin and human chromosomes New cases of XXY constitution in cattle. ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 2. CASTRATISM AND SO-CALLED KLINEFELTER'S SYNDROME AS DISEASE FORMS WITH KNOWN ETIOLOGY Medullary gonadal dysgenesis (chromatin-positive Klinefelter's syndrome); a genetically determined condition with eunuchoid measurements but early epiphyseal closure Paul Polani and the development of medical genetics Mechanisms of Non-Disjunction in Man
is cites work of	wds:Q34245719-7210D128-9074-4590-BF21-CA1F1263494C wds:Q64980495-880DF5C4-A7B1-4D23-8BBC-4414BD6AA0E8 wds:Q76666371-09CB9483-BF07-42ED-896A-7FDECF74055B wds:Q35745213-96ACAF1F-93D8-4A36-A1C2-3D5075707C53 wds:Q59082127-773D832F-1AD5-429C-A05B-5AECC75F5B1E wds:Q79404439-0C7018B9-45D4-4846-8E51-73BB0EA64E16 wds:Q35666920-14E64095-755B-43A4-BC02-5B9C6D8C9A52 wds:Q50351204-0DC1259F-DB2D-4960-B7A6-9C91C36CFEDF wds:Q58957250-1C4F70FE-F360-44E3-8657-270D591A7C2B wds:Q78705465-3AB9961B-B509-49E8-9EF9-0761F9758E05

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