(Q36059400)

11 August 2017

1 reference

title

Functional disomy of the Xq28 chromosome region (English)

1 reference

Nicole Morichon-Delvallez

11 August 2017

9

Nicole Morichon-Delvallez

0 references

Serge Romana

Serge Romana

13

0 references

Damien Sanlaville

Damien Sanlaville

1

0 references

Valérie Cormier-Daire

Valerie Cormier-Daire

11

0 references

Arnold Munnich

10

Arnold Munnich

1 reference

11 August 2017

14

Michel Vekemans

1 reference

11 August 2017

Marguerite Prieur

2

1 reference

11 August 2017

Marie-Christine de Blois

3

1 reference

11 August 2017

David Genevieve

4

1 reference

11 August 2017

Jean-Michel Lapierre

5

1 reference

11 August 2017

Catherine Ozilou

6

1 reference

11 August 2017

Monique Picq

7

1 reference

11 August 2017

Philippe Gosset

8

1 reference

11 August 2017

Nicole Morichon-Delvallez

9

1 reference

11 August 2017

Genevieve Baujat

12

1 reference

11 August 2017

Catherine Turleau

15

1 reference

11 August 2017

language of work or name

1 reference

1 May 2005

1 reference

European Journal of Human Genetics

11 August 2017

1 reference

11 August 2017

13

1 reference

11 August 2017

579-585

1 reference

11 August 2017

5

1 reference

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201384

11 August 2017

0 references

cites work

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

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/10.1038%2FSJ.EJHG.5201384

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

Functional disomy resulting from duplications of distal Xq in four unrelated patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

Disomy of distal Xq in males: case report and overview.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

Genome architecture, rearrangements and genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

Inherited duplication of Xq27.2-->qter: phenocopy of infantile Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201384

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201384

1 reference

Dimensions Publication ID

11 August 2017

0 references

1 reference