(Q33682115)

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Bilateral renal agenesis/hypoplasia/dysplasia (BRAHD): postmortem analysis of 45 cases with breakpoint mapping of two de novo translocations

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Bilateral renal agenesis/hypoplasia/dysplasia (BRAHD): postmortem analysis of 45 cases with breakpoint mapping of two de novo translocations (English)

1 reference

Europe PubMed Central

28 July 2017

Louise Harewood

object named as

Louise Harewood

1

0 references

David R. FitzPatrick

object named as

David R Fitzpatrick

9

0 references

author name string

Monica Liu

2

1 reference

Europe PubMed Central

28 July 2017

Jean Keeling

3

1 reference

Europe PubMed Central

28 July 2017

Alan Howatson

4

1 reference

Europe PubMed Central

28 July 2017

Margo Whiteford

5

1 reference

Europe PubMed Central

28 July 2017

Peter Branney

6

1 reference

Europe PubMed Central

28 July 2017

Margaret Evans

7

1 reference

Europe PubMed Central

28 July 2017

Judy Fantes

8

1 reference

Europe PubMed Central

28 July 2017

language of work or name

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publication date

25 August 2010

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

5

1 reference

Europe PubMed Central

28 July 2017

8

1 reference

Europe PubMed Central

28 July 2017

e12375

1 reference

Europe PubMed Central

28 July 2017

copyright license

Creative Commons Attribution 4.0 International

25 August 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Facial characteristics of infants with bilateral renal agenesis

1 reference

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21 June 2018

Renal cystic diseases in children: new concepts

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FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality

1 reference

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Renal aplasia in humans is associated with RET mutations

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A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman

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Müllerian anomalies

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Mutations in SOX2 cause anophthalmia

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Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes

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Strabismus (STB)/Vang-like (VANGL) gene family (Review)

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Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

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Classification of anorectal malformations--initial approach, diagnostic tests, and colostomy

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Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

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Heterogeneity of bilateral renal agenesis

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1 reference

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Bilateral renal agenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20811621

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FamiliaI aggregation in bilateral renal agenesis

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https://pubmed.ncbi.nlm.nih.gov/20811621

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1 reference

https://pubmed.ncbi.nlm.nih.gov/20811621

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1 reference

https://pubmed.ncbi.nlm.nih.gov/20811621

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Identifiers

10.1371/JOURNAL.PONE.0012375

1 reference

Europe PubMed Central

28 July 2017

2010PLoSO...512375H

0 references

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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