About: Identification of partial 12 trisomy by quinacrine fluorescence

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article by I A Uchida & C C Lin published 1 February 1973 in The Journal of Pediatrics

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття (uk) article by I A Uchida & C C Lin published 1 February 1973 in The Journal of Pediatrics (en)
publication date	wds:Q93732736-DFE19132-7336-4A6E-93FF-13C224E488FD
publication date	1973-02-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q93732736-8044E6C1-318A-406E-89B2-2F242EC098CA wds:Q93732736-9A462D80-8912-466B-9964-C9F0D8A4F940 wds:Q93732736-D22B6AA1-CE12-499B-B126-A9DCBA42D3D8 wds:Q93732736-EA7B6D39-7C1E-4520-94B2-B2C6CDFA9E8F wds:Q93732736-FCAB7026-A0BD-4BF5-A0F6-2DAB26053089
cites work	Dermatoglyphic nomogram for the diagnosis of Down's syndrome MATERNAL TRANSMISSION OF A NEW GROUP-C(6/9) CHROMOSOMAL SYNDROME MEIOTIC AND MITOTIC STUDIES OF A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN TWO AUTOSOMES OF GROUP 6-12 The use of dermal configurations in the diagnosis of mongolism A suggestion for the nomenclature of the fluorescent banding patterns in human metaphase chromosomes
author name string	wds:Q93732736-27F02E62-AC42-4C86-B6E6-833E7FF1C12A wds:Q93732736-F928EB06-EE2B-4F98-AE48-668B79A44DBB
author name string	C C Lin I A Uchida
rdfs:label	Identification of partial 12 trisomy by quinacrine fluorescence (en) Identification of partial 12 trisomy by quinacrine fluorescence (nl)
skos:prefLabel	Identification of partial 12 trisomy by quinacrine fluorescence (en) Identification of partial 12 trisomy by quinacrine fluorescence (nl)
name	Identification of partial 12 trisomy by quinacrine fluorescence (en) Identification of partial 12 trisomy by quinacrine fluorescence (nl)
title	wds:Q93732736-46202D55-CB92-46FA-9823-F25DC5243960
title	Identification of partial 12 trisomy by quinacrine fluorescence (en)
page(s)	wds:Q93732736-710F4ABB-2D6B-4588-86FC-71255EE151B5
page(s)	269-272
instance of	wds:Q93732736-5A3ACE5D-6400-42D2-9537-40D3903421CF
instance of	scholarly article
PubMed ID	wds:Q93732736-DD71CBFD-C50A-41A3-8A34-DC90F90AE09D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/4119313
PubMed ID	4119313
published in	wds:Q93732736-A2D9827F-BFBF-4609-B7DD-531F99177EA7
published in	The Journal of Pediatrics
issue	wds:Q93732736-91417E2F-1D4E-457F-BAE8-5B9F726F302C
volume	wds:Q93732736-3091C948-22B8-413C-A4B7-998CD5D3C5C5
issue	2
volume	82
DOI	wds:Q93732736-4409FA73-613A-4D70-A98E-E3538560EF07
DOI	http://dx.doi.org/10.1016/S0022-3476(73)80165-9
DOI	10.1016/S0022-3476(73)80165-9
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q93732736
is cites work of	Functional implications of differential chromosome banding Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13 A 21-21 tandem translocation with satellites on both long and short arms Two cases of 8p trisomy in one sibship Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis. Two cases of trisomy 12p due to rcpt(12;21)(p11;p11) inherited through three generations Cytogenetic and molecular analysis in trisomy 12p. Clinical and molecular cytogenetic observations in three cases of "trisomy 12p syndrome". De novo inverted tandem duplication of the short arm of chromosome 12 in a patient with microblepharon New chromosomal dysmorphic syndromes. 4. Trisomy 12p. Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother Trisomy 12p syndrome Evaluation of a family with a t(12;21)(p12.1;p11) translocation with unbalanced offspring Syndrome +12p. Case report and review Partial trisomy 12p due to t(12;21)pat translocation Trisomy 12p due to familial t(12p-,6q plus) translocation. Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome A newborn child with karyotype 47,XX,+der(12 (12pter leads to 12q12::9q24 leads to 8qter),t(8;12) (q24;q12) pat Translocations involving chromosome 12. I. A report of a 12,21 translocation in a woman with recurrent abortions, and a study of the breakpoints and modes of ascertainment of translocations involving chromosome 12 Trisomy 12p syndrome: de novo occurrence of mosaic trisomy 12p in a mentally retarded boy Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement? Trisomy 12p and epilepsy with myoclonic absences. Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21)
is cites work of	wds:Q33586216-31BDDAD1-4326-4827-A8F0-323255AB98EA wds:Q70943649-8775D0AC-E70A-43AF-9085-830FB0800550 wds:Q34464462-5F1258E0-ED1F-4A0C-9838-FCF51BC2AD99 wds:Q33586221-5B865BBB-D99D-4EEC-B139-A3DD75A7B05D wds:Q51926416-9DDF3BA1-D75F-45C0-B12C-62AA128BFD8B wds:Q39855253-216512AA-F68C-4FB9-971D-90159E6BA980 wds:Q41684080-38858E4B-D545-430F-8CF0-B397EA4E82A7 wds:Q48490211-65676082-A2C9-40B4-8C76-4DE8CFF902E3 wds:Q41045397-C486A460-1FF5-4F76-9942-2858C3F6A926 wds:Q52293147-41C1CFBA-640A-4AAA-B5A9-4BB45B8306DD wds:Q53721004-92C28937-7F7E-4800-8B35-61ECD724D6C7 wds:Q70018852-E4C0C23A-77E2-4F22-B5D6-9C318C523BF5 wds:Q36809358-CD749818-96FD-462E-A6A5-DF86773321F0 wds:Q41448883-556E7248-8677-439A-8B50-00F6A21D271E wds:Q73569784-FEBC3938-D946-4D40-99BB-520BA8821830 wds:Q67265542-FA05A97D-5773-4918-BF0F-A7125DAFEDC5 wds:Q44195777-E83FB0D2-1889-4664-B18A-F45973938117 wds:Q39344794-9AF77AF4-BD4B-4035-B9BF-9564AC60BD7A wds:Q41551957-32B15EA6-9E21-42EF-A771-6721DFDE62EF wds:Q53779220-F5DACF34-D98C-44F4-B2DE-993FE3903B1F wds:Q52114464-089E77EB-954A-41B7-AE7F-AEA124CAE538 wds:Q67556368-CA1BD97F-F818-4511-9CFC-2CC6E454BC15

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