About: A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT

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About: A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1963

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1963 (uk) im Dezember 1963 veröffentlichter wissenschaftlicher Artikel (de) 1963 թվականի դեկտեմբերի 1-ին հրատարակված գիտական հոդված (hy) artículu científicu espublizáu n'avientu de 1963 (ast) scientific article published on 01 December 1963 (en)
publication date	wds:Q76641784-899272C2-B973-4223-8BA4-C006B35B249A
publication date	1963-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q76641784-F3CF887D-5546-40E7-9BBA-2DB6F78E5459
language of work or name	English
cites work	wds:Q76641784-33416DA4-2150-4D49-BAF4-D7043396E860 wds:Q76641784-6E2CAD4C-8135-4EB4-B433-8D4B5BA3E605 wds:Q76641784-8D93BDC6-8C1D-47B8-ACF5-12CD5E32567D wds:Q76641784-C2BEA792-AC96-4D51-B309-D58BCFE5B08A wds:Q76641784-D859957F-BF27-4B44-8819-11F4D6BF6154
cites work	A child with 49 chromosomes Asynchronous duplication of human chromosomes and the origin of sex chromatin A case of XXXXY Klinefelter's syndrome A family with an XXXXY male, a leukaemic male, and two 21-trisomic mongoloid females The drumsticks of polymorphonuclear leucocytes in sex-chromosome abnormalities
author name string	wds:Q76641784-28BE5F05-1ADD-4346-9854-BA117C9DF666 wds:Q76641784-F1DBBCA2-FDA5-4FDA-B426-B531F0A91391
author name string	P V WOOLLEY N KESAREE
rdfs:label	A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT (en) A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT (nl)
skos:prefLabel	A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT (en) A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT (nl)
name	A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT (en) A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT (nl)
title	wds:Q76641784-78D5FEEE-E740-4AE4-B441-14C401A8D45A
title	A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT (en)
page(s)	wds:Q76641784-6A37B3F8-1975-4F61-AA85-A59B1D5D1476
page(s)	1099-1103
instance of	wds:Q76641784-48ECD855-EF30-4738-AC4B-114E22113054
instance of	scholarly article
main subject	wds:Q76641784-9BE22394-2C81-49E6-BF7F-012F0A2A6338
main subject	case report
PubMed ID	wds:Q76641784-9DEFC88D-76E3-4168-82B0-C52054EBA7BF
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14089814
PubMed ID	14089814
published in	wds:Q76641784-7071AA7E-DBF7-47E0-B412-5693C928E51B
published in	The Journal of Pediatrics
volume	wds:Q76641784-DCCD6D22-F47F-4841-ACB2-C3FEEFE9E0CA
volume	63
DOI	wds:Q76641784-F4AF5003-8246-4BA9-B154-9F5C375EEFE2
DOI	http://dx.doi.org/10.1016/S0022-3476(63)80190-0
DOI	10.1016/S0022-3476(63)80190-0
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q76641784
is cites work of	The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype. The XXXXY chromosome anomaly: report of three new cases and review of 30 cases from the literature SEX CHROMATIN. The triplo-X female: an appraisal based on a study of 12 cases and a review of the literature Detailed analysis of X chromosome inactivation in a 49,XXXXX pentasomy The penta-X syndrome A case of 49,XXXXX in which the extra X chromosomes were maternal in origin A new case of prenatally diagnosed pentasomy x: review of the literature X pentasomy: A case and review A case of quintuple-X syndrome (49,XXXXX) A female child with five X chromosomes Letter: Food: influence of form on absorption The 49,XXXXX chromosome constitution: similarities to the 49,XXXXY condition Letter: Pentasomy of X chromosome THE XXXXY SYNDROME. A REPORT OF A CASE AND REVIEW OF THE LITERATURE. Sex Chromosomes and Sex Chromatin The Significance of the Sex Chromatin* Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism HUMAN AND ANIMAL CHROMOSOMES. SEX CHROMATIN. Tetrasomy and pentasomy of the X chromosome. Atrial Septal Defect Associated with Skeletal Anomalies (Holt-Oram Syndrome) THE CHROMOSOMES--AN INTRODUCTION--WITH SOME OBSERVATIONS IN INDIAN CHILDREN Report of a new case with pentasomy X and novel clinical findings A case of penta X syndrome caused by nondisjunction in maternal meiosis 1 and 2. Recent advances in investigation and treatment of infertility
is cites work of	wds:Q35075233-D984EAD6-C0CD-406B-8D04-903258953F7B wds:Q39356791-2A3E5D1E-BD5A-4AB6-AAEE-6A037DE4DDF6 wds:Q35936054-6E9BF1DA-3415-4F14-ACC0-1F31886312D9 wds:Q34634360-52E518D7-BA74-4693-8554-7306A0367D02 wds:Q35853907-E81CF66F-DB34-4F10-B469-1C33DEC3DBA3 wds:Q71696117-84D037A0-B46B-4622-BB77-D3D681B91E68 wds:Q24672599-F1F20CFA-4B64-4A16-B3C7-F81CBBF7C1B8 wds:Q36623507-B9AE9AFD-2250-44E2-ABA8-5939D6121C73 wds:Q51462172-68F3065E-0C6F-4D55-A9D8-7017B83CCEE6 wds:Q21092940-C7CFDD39-59E2-4530-947E-B2E1FC5EC176 wds:Q24517830-049A28B8-9F01-4490-B859-8E5E851092C9 wds:Q39356786-0E8408A1-F877-4C32-8A88-9850B0E567BA wds:Q44510380-0362F751-C088-44AF-923D-57973EEBB40B wds:Q35414016-8BC44409-FA4B-4578-A6BB-EAEF730C8364 wds:Q71748569-8ACB2F2D-2DAF-4848-A7BD-133AC9865DAE wds:Q72200674-6575340C-74EA-4572-B3C8-5F876CE4E8D2 wds:Q33584789-E6B884AF-FD5B-4BE5-B869-2F9EE84C9E68 wds:Q33863203-5D6983AD-1439-4340-B2B4-D443EFFA1FFF wds:Q35936224-0CB9EE89-DDB5-4197-8138-BC928DDB5AFF wds:Q40024753-9CC7C88D-F5E0-41B6-AD2E-9D8341800A3D wds:Q58964536-8BC6EA2F-3D21-4FCC-85CC-C2D51A83BD47 wds:Q76901896-B3C80987-93A3-4567-A1C5-EB4544C35FC6 wds:Q35917894-D9460BF9-A758-479C-BC65-05DC07D2E216 wds:Q40047612-03E9F3BD-95EF-4AE6-85B6-164196943C88 wds:Q48010037-4140C02C-39AB-40D5-8AAE-EE385E15C667

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