(Q34176490)

31 July 2017

1 reference

title

Functional disomy for Xq26.3-qter in a boy with an unbalanced t(X;21)(q26.3;p11.2) translocation (English)

1 reference

31 July 2017

Akiyama M

1

1 reference

31 July 2017

Kawame H

2

1 reference

31 July 2017

Ohashi H

3

1 reference

31 July 2017

Tohma T

4

1 reference

31 July 2017

Ohta H

5

1 reference

31 July 2017

Shishikura A

6

1 reference

31 July 2017

Miyata I

7

1 reference

31 July 2017

Usui N

8

1 reference

31 July 2017

Eto Y

9

1 reference

31 July 2017

publication date

1 March 2001

1 reference

American Journal of Medical Genetics Part A

31 July 2017

published in

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31 July 2017

volume

99

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31 July 2017

issue

2

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31 July 2017

page(s)

111-114

1 reference

Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated families.

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%282001%299999%3A9999%3C%3A%3AAID-AJMG1150%3E3.0.CO%3B2-C

Cytogenetic and molecular studies on a recombinant human X chromosome: implications for the spreading of X chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%282001%299999%3A9999%3C%3A%3AAID-AJMG1150%3E3.0.CO%3B2-C

Functional disomies of the X chromosome influence the cell selection and hence the X inactivation pattern in females with balanced X-autosome translocations: A review of 122 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%282001%299999%3A9999%3C%3A%3AAID-AJMG1150%3E3.0.CO%3B2-C

Inherited inverted duplication of X chromosome in a male: report of a patient and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%282001%299999%3A9999%3C%3A%3AAID-AJMG1150%3E3.0.CO%3B2-C

A new syndrome with mental retardation, short stature and an Xq duplication.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%282001%299999%3A9999%3C%3A%3AAID-AJMG1150%3E3.0.CO%3B2-C

A familial Xp+ chromosome, dup (Xq26.3-->qter).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%282001%299999%3A9999%3C%3A%3AAID-AJMG1150%3E3.0.CO%3B2-C

Growth hormone deficiency and empty sella syndrome in a boy with dup(X) (q13.3----q21.2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%282001%299999%3A9999%3C%3A%3AAID-AJMG1150%3E3.0.CO%3B2-C

10.1002/1096-8628(2001)9999:9999<::AID-AJMG1150>3.0.CO;2-C

21 January 2018

Identifiers

DOI

1 reference

31 July 2017

1 reference