Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis - Wikidata - awgldk - TriplyDB

Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis

Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis

http://www.wikidata.org/entity/Q33596221

about

Prenatal findings in trisomy 16q of paternal origin.Congenital knee dislocation in a 49,XXXXY boy A rare non-Robertsonian translocation involving chromosomes 15 and 21.Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.Transient neonatal hypothyroidism in a boy with unbalanced translocation t(8;16).Investigation of a patient with a partial trisomy 16q including the fat mass and obesity associated gene (FTO): fine mapping and FTO gene expression study.Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: Case report and review of literature

P2860

Q33653179-685A6DCB-31DB-45BE-8B73-3A74AD54B71E Q33676426-E7A246FA-AC6F-47B7-8A69-0AF8DE7A6C0B Q44031565-E7B28EA8-438A-446B-B316-F13392263A33 Q47371331-B033617D-FCBA-4C1D-9F90-22F5533A1780 Q50728748-55B07391-435B-4286-AAC7-0E6EC3379552 Q54439756-845ACB3F-4711-4043-83AE-992DE42BC94F Q57790305-6D7B2826-BB80-4B28-8FD5-D5D444B9B9B1

P2860

Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis

http://www.wikidata.org/entity/Q33596221

description

1994 nî lūn-bûn

@nan

1994 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

1994 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

1994年の論文

@ja

1994年論文

@yue

1994年論文

@zh-hant

1994年論文

@zh-hk

1994年論文

@zh-mo

1994年論文

@zh-tw

1994年论文

@wuu

name

Duplication of 16q22-->qter co ...... isation and molecular analysis

@ast

Duplication of 16q22-->qter co ...... isation and molecular analysis

@en

type

label

Duplication of 16q22-->qter co ...... isation and molecular analysis

@ast

Duplication of 16q22-->qter co ...... isation and molecular analysis

@en

prefLabel

Duplication of 16q22-->qter co ...... isation and molecular analysis

@ast

Duplication of 16q22-->qter co ...... isation and molecular analysis

@en

P1433

Q33596221-2BEA7F88-503F-477F-9FED-BBEBBE66A570

P1476

Q33596221-0ECF9425-41AB-49D7-A539-B67028390B80

P2093

Q33596221-39CBF544-2ED6-4B06-8DD9-E4164BEDF787

Q33596221-48007519-9156-4740-B1EB-AFE1C8B70BF9

Q33596221-64C2F53B-A15E-4AD4-ACF9-8901A2268BEB

Q33596221-A77D5BB7-49D6-49ED-84B6-41CF34DA3708

Q33596221-E3962D03-AA11-4ACC-8DF1-6AB3E357630C

P2860

Q33596221-33A1AF3E-C6A2-4741-9B0E-95116B1B1C2B

Q33596221-477B6AD7-35A3-49A0-A5A7-19BEDCB7A70C

Q33596221-4C306BB0-2D16-4FBF-ACDE-A88E0FD49C08

Q33596221-56841BF0-4632-4FCE-B654-7A607DA66AAC

Q33596221-589EEF93-6BC3-4DC0-A9E1-8600E86E307E

Q33596221-80E506D9-E1CE-473D-B724-EB69E1EA0FC4

Q33596221-A17AF80F-E622-4791-8D46-2334B0927878

Q33596221-AA901349-FB53-4571-8EEB-6BBD9B79DE23

Q33596221-B8803993-4557-4004-8549-BE75B6B1C4C6

Q33596221-D6202BC7-E897-421C-8AEA-D19955D11D65

P304

Q33596221-FC46D3C4-93B8-4C62-B0C0-8E9A16035AE5

P31

Q33596221-3D553D4A-E4EB-442D-A967-16EF3DCE1EC1

P356

Q33596221-4238D75B-2F66-46B0-BB85-D60D6AAC9547

P407

Q33596221-ECC0535E-9F64-401A-AE85-5A62F3879331

P433

Q33596221-0604E0BE-DCD1-47E3-AA70-12263ACF776F

P478

Q33596221-9C4B5149-32B3-484D-91E1-449F2EA768B6

P577

Q33596221-E296D5B3-9B53-4597-8EA1-791E2B832889

P5875

Q33596221-12BA0E6B-5534-4254-9E66-1C4E440CC91C

P698

Q33596221-F17D6A48-180C-4ED6-8131-F42052474FDD

P932

Q33596221-4732BD85-BC0D-42C5-A1F5-1BC8DD2AF3E4

P356

P1433

Journal of Medical Genetics

P1476

Duplication of 16q22-->qter co ...... isation and molecular analysis

@en

P2093

I K Temple

http://www.w3.org/2001/XMLSchema#string

R Ironton

http://www.w3.org/2001/XMLSchema#string

R M Renshaw

http://www.w3.org/2001/XMLSchema#string

R S Houlston

http://www.w3.org/2001/XMLSchema#string

R S James

http://www.w3.org/2001/XMLSchema#string

P2860

A second-generation linkage map of the human genome.

Trisomy 16q arising from a maternal 15p;16q translocation.

Partial trisomy for long arm of chromosome 16.

Partial trisomy 16 as a result of familial 16;20 translocation.

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.

Partial duplication 16q: report of two affected siblings resulting from a maternal translocation and literature review.

Partial trisomy 16q resulting from maternal translocation.

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms.

P304

884-887

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1136/JMG.31.11.884

http://www.w3.org/2001/XMLSchema#string

P407

P433

11

http://www.w3.org/2001/XMLSchema#string

P478

31

http://www.w3.org/2001/XMLSchema#string

P577

1994-11-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

15346603

http://www.w3.org/2001/XMLSchema#string

P698

7853376

http://www.w3.org/2001/XMLSchema#string

P932

1016665

http://www.w3.org/2001/XMLSchema#string