(Q33687755)

28 July 2017

1 reference

title

Ring 2 chromosome: ten-year follow-up report (English)

1 reference

28 July 2017

Lacassie Y

1

1 reference

28 July 2017

Arriaza MI

series ordinal

2

1 reference

28 July 2017

Vargas A

series ordinal

3

1 reference

28 July 2017

La Motta I

series ordinal

4

1 reference

28 July 2017

publication date

1 July 1999

1 reference

American Journal of Medical Genetics Part A

28 July 2017

published in

1 reference

28 July 2017

volume

85

1 reference

28 July 2017

issue

2

1 reference

28 July 2017

page(s)

117-122

1 reference

Small terminal deletions of the long arm of chromosome 2: two new cases.

28 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

Ring chromosome 2: clinical, chromosomal, and biochemical aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

Three cases of ring chromosome 2, one derived from a paternal 2/6 translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchange.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

Clinical phenotype associated with terminal 2q37 deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

Does "ring syndrome" exist? An analysis of 207 case reports on patients with a ring autosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

Ring chromosome 2 in a child with growth failure and few congenital abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

Ring chromosome and latent centromeres

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990716%2985%3A2%3C117%3A%3AAID-AJMG4%3E3.0.CO%3B2-O

10.1002/(SICI)1096-8628(19990716)85:2<117::AID-AJMG4>3.0.CO;2-O

21 January 2018

Identifiers

DOI

1 reference

28 July 2017

1 reference