(Q57655070)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24764164%20AND%20SRC:MED&resulttype=core&format=json

15 March 2020

title

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24764164%20AND%20SRC:MED&resulttype=core&format=json

15 March 2020

1 reference

1

1 reference

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15 March 2020

Martin Kerick

5

1 reference

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15 March 2020

Stefan Herms

15

1 reference

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15 March 2020

Agneta Nordenskjöld

21

1 reference

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15 March 2020

Bernhard Herrmann

23

1 reference

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15 March 2020

Markus M Nöthen

24

1 reference

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15 March 2020

16

John P Gearhart

1 reference

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15 March 2020

author name string

Friederike Baudisch

2

1 reference

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15 March 2020

Bernd Timmermann

3

1 reference

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15 March 2020

Heiner Kuhl

4

1 reference

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15 March 2020

Judith Proske

6

1 reference

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15 March 2020

Lars Wittler

7

1 reference

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15 March 2020

Tracie Pennimpede

8

1 reference

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15 March 2020

Anne-Karoline Ebert

9

1 reference

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15 March 2020

Wolfgang Rösch

10

1 reference

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15 March 2020

Raimund Stein

11

1 reference

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15 March 2020

Enrika Bartels

12

1 reference

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15 March 2020

Catharina von Lowtzow

13

1 reference

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15 March 2020

Yegappan Lakshmanan

17

1 reference

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15 March 2020

Christina Clementsson Kockum

18

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15 March 2020

Gundela Holmdahl

19

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15 March 2020

Göran Läckgren

20

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15 March 2020

Michael Ludwig

25

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15 March 2020

Heiko Reutter

26

1 reference

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15 March 2020

Thomas M Boemers

14

1 reference

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15 March 2020

Simeon A Boyadjiev

22

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15 March 2020

publication date

25 April 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24764164%20AND%20SRC:MED&resulttype=core&format=json

Birth Defects Research Part A: Clinical and Molecular Teratology

15 March 2020

published in

1 reference

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15 March 2020

volume

100

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15 March 2020

issue

6

1 reference

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15 March 2020

page(s)

512-517

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24764164%20AND%20SRC:MED&resulttype=core&format=json

22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome

15 March 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

The exstrophy-epispadias complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

A common molecular basis for rearrangement disorders on chromosome 22q11

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

GUDMAP: the genitourinary developmental molecular anatomy project

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

In vivo knockdown of Brachyury results in skeletal defects and urorectal malformations resembling caudal regression syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

Microduplication 22q11.2: a new chromosomal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

Molecular mechanisms for constitutional chromosomal rearrangements in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

GenePaint.org: an atlas of gene expression patterns in the mouse embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

Insertion/deletion polymorphisms in the ΔNp63 promoter are a risk factor for bladder exstrophy epispadias complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.23249

21 January 2018

Identifiers

DOI

10.1002/BDRA.23249

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24764164%20AND%20SRC:MED&resulttype=core&format=json

15 March 2020

1 reference