(Q38505070)

3 September 2017

Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousins (English)

1 reference

3 September 2017

4

Semenza GL

1 reference

3 September 2017

Doheny KF

1

1 reference

3 September 2017

Rasmussen SA

2

1 reference

3 September 2017

Rutberg J

3

1 reference

3 September 2017

Stamberg J

5

1 reference

3 September 2017

Schwartz M

6

1 reference

3 September 2017

Batista DA

7

1 reference

3 September 2017

Stetten G

8

1 reference

3 September 2017

Thomas GH

9

1 reference

3 September 2017

1 March 1997

1 reference

American Journal of Medical Genetics Part A

3 September 2017

1 reference

3 September 2017

69

1 reference

3 September 2017

188-193

1 reference

3 September 2017

2

1 reference

Insertional translocations: report of two new families and review of the literature

3 September 2017

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

Molecular analysis of a complex chromosomal rearrangement and a review of familial cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

A new case of proximal 10q partial trisomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

Apparent late-onset Cockayne syndrome and interstitial deletion of the long arm of chromosome 10 (del(10)(q11.23q21.2))

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

Duplication and deletion of chromosome band 2(p21p22) resulting from a familial interstitial insertion (2;11)(p21;p15).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970317%2969%3A2%3C188%3A%3AAID-AJMG14%3E3.0.CO%3B2-H

Tandem duplication of 10(q21-q22) in a mentally deficient man

21 January 2018

0 references

Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22)

0 references

Diagnosis of microdeletion syndromes: high-resolution chromosome analysis versus fluorescence in situ hybridization

0 references

Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3)

0 references

FISH analysis in Prader-Willi and Angelman syndrome patients

0 references

Proximal duplication of the long arm of chromosome 10 (10q11.2----10q22): a distinct clinical entity

0 references

Familial mental retardation in a family with an inherited chromosome rearrangement.

0 references

De novo 10q(q21q22) interstitial deletion

0 references

Serial duplication of 10 (q21?q22) in a mentally retarded boy with congenital malformations

0 references

Identifiers

DOI

10.1002/(SICI)1096-8628(19970317)69:2<188::AID-AJMG14>3.0.CO;2-H

1 reference

release_cxxr7uy7f5gqpcukq5duypoa3e

3 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/cxxr7uy7f5gqpcukq5duypoa3e

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference