(Q38507726)

English

Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality

scientific article published on January 1996

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scholarly article

1 reference

Europe PubMed Central

3 September 2017

Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality (English)

1 reference

Europe PubMed Central

3 September 2017

author name string

Tonk V

1

1 reference

Europe PubMed Central

3 September 2017

Schneider NR

2

1 reference

Europe PubMed Central

3 September 2017

Delgado MR

3

1 reference

Europe PubMed Central

3 September 2017

Mao J

4

1 reference

Europe PubMed Central

3 September 2017

Schultz RA

5

1 reference

Europe PubMed Central

3 September 2017

publication date

1 January 1996

1 reference

Europe PubMed Central

3 September 2017

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

3 September 2017

61

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Europe PubMed Central

3 September 2017

16-20

1 reference

Europe PubMed Central

3 September 2017

1

1 reference

Europe PubMed Central

3 September 2017

Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

A new case of proximal 10q partial trisomy

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Partial trisomy 10q: a recognizable syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Transmission of ring 14 chromosome from mother to two sons

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Parental mosaicism as a cause of Down syndrome. A report of 46,XX/46,XX,--21,+t(21q21q1 mother and 46,XY,+21,+t(21q21q) child

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Confirmation of a de novo duplication, dup(10)(q24 leads to q26), by GOT1 gene dosage studies.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

High Resolution of Human Chromosomes

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Development of 124 sequence-tagged sites and cytogenetic localization of 217 cosmids for human chromosome 10.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Isochromosome 18p in a mother and her child

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Duplication 10q confirmed by DNA in situ hybridization

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Ocular findings in partial trisomy 10q syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

A rapid banding technique for human chromosomes

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C16%3A%3AAID-AJMG3%3E3.0.CO%3B2-V

21 January 2018

Identifiers

10.1002/(SICI)1096-8628(19960102)61:1<16::AID-AJMG3>3.0.CO;2-V

1 reference

Europe PubMed Central

3 September 2017

1 reference

Europe PubMed Central

3 September 2017

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