(Q41453528)

30 September 2017

1 reference

title

A case of presumptive monosomy 21 re-diagnosed as unbalanced t(5p;21q) by FISH and review of literature (English)

1 reference

30 September 2017

1 reference

Iqbal MA

1

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30 September 2017

Ahmed MZ

series ordinal

2

1 reference

30 September 2017

Wu D

series ordinal

3

1 reference

30 September 2017

Sakati N

series ordinal

4

1 reference

30 September 2017

language of work or name

1 reference

1 May 1997

1 reference

American Journal of Medical Genetics Part A

30 September 2017

published in

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30 September 2017

volume

70

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30 September 2017

issue

2

1 reference

30 September 2017

page(s)

174-178

1 reference

describes a project that uses

30 September 2017

fluorescence in situ hybridization

1 reference

based on heuristic

inferred from title

cites work

Full monosomy 21: a clinically recognizable syndrome?

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

Fetal t(5p;21q) misdiagnosed as monosomy 21: a plea for in situ hybridization studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

Unbalanced 13q/21q translocation: a revised study of the case previously reported as 21-monosomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

A child with presumptive monosomy 21 (45,XY,-21) in a family in which some members are Gq-

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

Monosomy 21: A possible stepwise evolution of the karyotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

A female infant with monosomy 21

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

21 monosomy in a retarded female infant

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

De novo t(5p;21q) in a patient previously diagnosed as monosomy 21

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

Letter: Does full monosomy 21 exist? A comment to the paper: A male infant with monosomy 21 by Y. Kaneko, T. Ikeuchi, M. Sasaki, Y. Satake and S. Kuwajima Humangenetik 29, 1-7 (1975)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970516%2970%3A2%3C174%3A%3AAID-AJMG14%3E3.0.CO%3B2-G

10.1002/(SICI)1096-8628(19970516)70:2<174::AID-AJMG14>3.0.CO;2-G

21 January 2018

Identifiers

DOI

1 reference

30 September 2017

1 reference