About: Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism

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About: Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 1962

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) artículo científico publicado en 1962 (es) artigo científico (publicado na 1962) (pt) наукова стаття, опублікована в січні 1962 (uk) article scientifique publié en 1962 (fr) artikull shkencor i botuar më 01 janar 1962 (sq) scientific article published on 01 January 1962 (en) 1962 թվականի հունվարի 1-ին հրատարակված գիտական հոդված (hy) artículu científicu espublizáu en xineru de 1962 (ast)
publication date	wds:Q79400280-127A200E-FDDC-468F-BBBC-3AC327028FF8
publication date	1962-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q79400280-D73BFAD9-61F8-4AB6-BE11-45D99ED2C6BF
language of work or name	English
cites work	wds:Q79400280-43B7DA97-DF3C-4126-986A-8503A34FD244 wds:Q79400280-9E2978AE-892B-43E6-A383-B8E8B3D571F8 wds:Q79400280-AEA2693D-B374-4B89-87C2-A7435D28EB9F wds:Q79400280-D7E2F3EF-7D3C-43D3-9527-F1A90CBEC109
cites work	Chromosomal translocations in mongolism and in normal relatives Chromosomal abnormalities in father and Mongol child Chromosome preparations of leukocytes cultured from human peripheral blood Chromosome studies in detection of parents with high risk of second child with Down's syndrome
author name string	wds:Q79400280-467B5BB4-FC8C-4A48-9B2D-8E432AD74079 wds:Q79400280-B263A17C-BEB9-4C09-A69A-70DA80718F43 wds:Q79400280-C3E76A44-0B10-47F4-A29A-0EB4C65740AF
author name string	D W ASHBY J E GRAY D E MUTTON
rdfs:label	Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (en) Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (nl) Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (sq)
skos:prefLabel	Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (en) Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (nl) Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (sq)
name	Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (en) Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (nl) Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (sq)
title	wds:Q79400280-50F3283A-0B7A-4F49-B518-36F8E4300874
title	Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism (en)
page(s)	wds:Q79400280-29035326-EE64-4D65-87D2-1AB69DDEED99
page(s)	21-23
instance of	wds:Q79400280-AB8E9339-D3D1-47DC-8162-380093101EEF
instance of	scholarly article
PubMed ID	wds:Q79400280-813F1470-0523-4DD7-866D-033CB78FA416
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13901315
PubMed ID	13901315
published in	wds:Q79400280-B858520E-9AED-4E24-B58E-8B75177079AB
published in	The Lancet
issue	wds:Q79400280-57745733-ADB5-4A31-AEE4-D41AB16037F4
volume	wds:Q79400280-F180DD53-FE61-431D-A015-E1B659B50A7C
issue	7219
volume	1
DOI	wds:Q79400280-9043C63E-2088-4D0E-BCC5-45B1E02E8908
DOI	http://dx.doi.org/10.1016/S0140-6736(62)92643-0
DOI	10.1016/S0140-6736(62)92643-0
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q79400280
is cites work of	Pericentric inversion in a group D chromosome (13?15) associated with amenorrhea and gonadal dysgenesis An unusual translocation in a case of Mongolism Short arm enlargement in acrocentric chromosomes. Maternal transmission of a 21/1 translocation associated with Down's syndrome CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRIS Inherited pericentric inversion of chromosome no. 4. Paternal age in mongolism FAMILIAL DOWN'S SYNDROME WITH UNDETECTED TRANSLOCATION Pericentric inversions. Problems and significance for clinical genetics The chromosome complement of the aardvark, Orycteropus afer DE LANGE SYNDROME. THE "AMSTERDAM TYPE" OF MENTAL DEFECT WITH CONGENITAL MALFORMATION. THYROID FUNCTION IN MONGOLISM. Patau's syndrome with D1 duplication‐deficiency derived from a maternal D group pericentric inversion A MONGOL WITH A 21:22 TYPE CHROMOSOMAL TRANSLOCATION Familial transmission of an aberrant submetacentric chromosome A 13-15/21 translocation chromosome in carrier father and mongol son. The chromosome abnormality in mongolism A further example of familial Gp+ associated with trisomy G A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21 TRIPLE STEM-LINE CHROMOSOMAL MOSAICISM IN DOWN'S SYNDROME (MONGOLISM) Short arm enlargement in a G chromosome MONGOLISM (DOWN'S SYNDROME) WITH ATYPICAL CLINICAL AND CYTOGENETIC FEATURES Down's syndrome with an unusual karyotype. Cytogenetic Study of Otosclerosis To the genetics and clinical aspects of small chromosome aberrations. A chromosome Gp-h and a chromosome Gs- in one family A Rare Case of Pericentric Inversion, Inv (21) (p12;q22) in Repeated Pregnancy Loss: A Case Report
is cites work of	wds:Q68385819-9A9FF265-4382-4711-85E9-3C5B8CCE6426 wds:Q76626967-3716DA06-E067-4197-BD48-7893323811FC wds:Q35232381-33D7CD6C-A610-4091-9565-5B58334B673A wds:Q35744548-E326DE6E-BBE2-401B-A988-4C8F8F6492E0 wds:Q71978156-32CC858C-087A-4376-9329-43F1F6224C56 wds:Q73895421-1467BE8D-9EDD-48B9-9019-133EBE69DF1A wds:Q76413738-5EE9A0C5-58B9-4D83-AB79-541A6CD8D85B wds:Q52132594-7E6F1C41-BEBC-440E-B78C-9A43D46D8889 wds:Q68427440-51B248E6-87B8-4976-85DA-7A5BB997C64F wds:Q71615989-05D67DF0-5A5B-4113-8E9E-0A5A987FAEEE wds:Q34633019-55C3652B-823F-4B09-9C70-5689595DFF1E wds:Q72072955-5557D298-CA9A-419E-B768-849B3DE37894 wds:Q76925371-DAB42D15-74BF-4433-B192-374C48FF1D26 wds:Q77170076-E1C6127D-5F14-4DB6-BB8B-EB74A56DDB27 wds:Q35651551-5E9E8BF9-8F9B-4655-86E2-C90C4FF51B79 wds:Q51283214-A52B0B6F-3739-41C9-B7E5-1D03A3BCBA6F wds:Q70566104-CBBC1FE3-518B-42CA-9017-EF194D31F8D9 wds:Q35744771-DB5555B7-AE61-4055-A8DB-5E88592A3AA5

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