(Q34357387)

1 August 2017

A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10. (English)

1 reference

1 August 2017

4

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1 August 2017

Giuseppe Martucciello

object named as

Martucciello G

9

0 references

Arnold Munnich

15

object named as

Munnich A

1 reference

1 August 2017

Lyonnet S

1

1 reference

1 August 2017

Bolino A

2

1 reference

1 August 2017

Pelet A

3

1 reference

1 August 2017

Nihoul-Fékété C

5

1 reference

1 August 2017

Briard ML

6

1 reference

1 August 2017

Mok-Siu V

7

1 reference

1 August 2017

Kaariainen H

8

1 reference

1 August 2017

Lerone M

10

1 reference

1 August 2017

Puliti A

11

1 reference

1 August 2017

Luo Y

12

1 reference

1 August 2017

Weissenbach J

13

1 reference

1 August 2017

Devoto M

14

1 reference

1 August 2017

Romeo G

16

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1 August 2017

language of work or name

English

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publication date

1 August 1993

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1 August 2017

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1 August 2017

4

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1 August 2017

346-350

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1 August 2017

4

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https://scigraph.springernature.com/pub.10.1038/ng0893-346

1 August 2017

0 references

cites work

The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families.

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

Quantitative and qualitative analysis of the extracellular matrix protein, laminin, in Hirschsprung's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

Hirschsprung disease in a large birth cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

An Epidemiological Study of Hirschsprung's Disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Adult-Onset Hirschsprung's Disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Hirschsprung's disease in a kindred: A possible clue to the genetics of the disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Three-generation transmission of Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Familial Aspects of Hirschsprung's Disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

The association of Waardenburg syndrome and Hirschsprung megacolon

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Hirschsprung disease in a 46,XY phenotypic infant girl with Smith-Lemli-Opitz syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

MONGOLISM ASSOCIATED WITH HIRSCHSPRUNG'S DISEASE

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Association of Megacolon with Two Recessive Spotting Genes in the Mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Association of megacolon with a new dominant spotting gene (Dom) in the mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Aganglionosis in rodents

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

A primary genetic map of markers of human chromosome 10

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Waardenburg's syndrome with Hirschsprung's disease: a neural crest defect

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Total colonic aganglionosis (Zuelzer-Wilson syndrome) and congenital failure of automatic control of ventilation (Ondine's curse).

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Hirschsprung's disease in a family with multiple endocrine neoplasia type 2.

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Multiple endocrine neoplasia type II B with symptoms suggesting Hirschsprung's disease: a case report

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Multifocal ganglioneuroblastoma coexistent with total colonic aganglionosis

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Localization of a 900-bp-long fragment of the human choline acetyltransferase gene to 10q11.2 by nonradioactive in situ hybridization

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Total colonic aganglionosis (with or without ileal involvement): a review of 27 cases

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Deleted and normal chromosome 10 homologs from a patient with Hirschsprung disease isolated in two cell hybrids through enrichment by immunomagnetic selection

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-346

7 January 2021

Identifiers

DOI

10.1038/NG0893-346

1 reference

1 August 2017

1 reference