(Q52130478)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

Xp22.3; Yq11.2 chromosome translocation and its clinical manifestations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1

1 reference

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10 November 2019

author name string

J Fryns

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

L Lagae

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

M Syrrou

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

P Marynen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

K Devriendt

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

publication date

1 April 2001

1 reference

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10 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

44

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

71-76

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

Molecular heterogeneity of steroid sulfatase deficiency: A multicenter study on 57 unrelated patients, at DNA and protein levels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

X;Y translocation in an adolescent mentally normal phenotypic male with features of hypogonadism.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

Development and physical analysis of YAC contigs covering 7 Mb of Xp22.3-p22.2.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

The IL-9 receptor gene (IL9R): genomic structure, chromosomal localization in the pseudoautosomal region of the long arm of the sex chromosomes, and identification of IL9R pseudogenes at 9qter, 10pter, 16pter, and 18pter

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

Schizophrenia susceptibility gene locus at Xp22.3.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

Y to X translocation in man

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

X/Y translocations resulting from recombination between homologous sequences on Xp and Yq.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2801%2901071-1

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0003-3995(01)01071-1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11522244%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference