(Q34357393)

1 August 2017

title

A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10. (English)

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1 August 2017

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9

Reyna T

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author name string

Angrist M

1

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1 August 2017

Kauffman E

2

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1 August 2017

Slaugenhaupt SA

3

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1 August 2017

Matise TC

4

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1 August 2017

Puffenberger EG

5

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1 August 2017

Washington SS

6

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1 August 2017

Lipson A

7

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1 August 2017

Cass DT

8

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1 August 2017

Weeks DE

10

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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

volume

4

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1 August 2017

issue

4

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1 August 2017

page(s)

351-356

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

1 August 2017

cites work

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The neurofibromatosis type 1 gene encodes a protein related to GAP

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An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

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Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

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A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

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Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

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My early experience with Hirschsprung's disease

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Three-generation transmission of Hirschsprung's disease

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Three-generation transmission of Hirschsprung's disease

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7 January 2021

Association of Megacolon with Two Recessive Spotting Genes in the Mouse

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7 January 2021

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

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7 January 2021

Gastrointestinal manifestations of Sipple syndrome in children

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

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

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

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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

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7 January 2021

Linkage mapping of human chromosome 10 microsatellite polymorphisms

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Dinucleotide repeat polymorphism at the RBP3 locus in chromosome band 10q11.2

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A 40-year multinational retrospective study of 880 Swenson procedures.

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Long-segment Hirschsprung's disease

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Pre- and postnatal development of the ganglion cells of the rectum and its surgical implications

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7 January 2021

Identification of the neurofibromatosis type 1 gene product

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Aganglionosis: associated anomalies

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

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Evidence that enteric neurons may derive from the sympathoadrenal lineage

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7 January 2021

Cell fate determination in the peripheral nervous system: the sympathoadrenal progenitor

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Mammalian achaete-scute homolog 1 is transiently expressed by spatially restricted subsets of early neuroepithelial and neural crest cells

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New blossoms in the neural crest field: trophic and transcription factors

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The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies

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7 January 2021

Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11-q21

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7 January 2021

Identification and characterization of a gene at D10S94 in the MEN2A region

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7 January 2021

A cluster of expressed zinc finger protein genes in the pericentromeric region of human chromosome 10.

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7 January 2021

Construction of multilocus genetic linkage maps in humans

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7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

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7 January 2021

Strategies for multilocus linkage analysis in humans

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7 January 2021

Identifiers

DOI

10.1038/NG0893-351

1 reference

release_6j6zkxbgwzbhfmispylhxb6iiq

1 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6j6zkxbgwzbhfmispylhxb6iiq

24 November 2022

mapped directly with Wikidata item

1 reference