(Q36708731)

15 August 2017

Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family (English)

1 reference

15 August 2017

1 reference

F A Hol

1

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15 August 2017

B C Hamel

2

1 reference

15 August 2017

M P Geurds

3

1 reference

15 August 2017

I Hansmann

4

1 reference

15 August 2017

F A Nabben

5

1 reference

15 August 2017

O Daniëls

6

1 reference

15 August 2017

E C Mariman

7

1 reference

15 August 2017

1 June 1995

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15 August 2017

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15 August 2017

95

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15 August 2017

6

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15 August 2017

687-690

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https://scigraph.springernature.com/pub.10.1007/bf00209488

15 August 2017

0 references

cites work

Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH)

1 reference

12 December 2020

Del(20p) with manifestations of arteriohepatic dysplasia

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12 December 2020

The Alagille syndrome (arteriohepatic dysplasia).

1 reference

12 December 2020

Alagille syndrome and deletion of 20p.

1 reference

12 December 2020

Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2)

1 reference

12 December 2020

Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome)

1 reference

12 December 2020

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers

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12 December 2020

Segregation analysis of Alagille syndrome

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12 December 2020

Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)

1 reference

12 December 2020

Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur

1 reference

12 December 2020

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases

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12 December 2020

The role of Pax-1 in axial skeleton development.

1 reference

12 December 2020

Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies.

1 reference

12 December 2020

Pax 1, a member of a paired box homologous murine gene family, is expressed in segmented structures during development

1 reference

12 December 2020

The 1993-94 Généthon human genetic linkage map

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12 December 2020

Arteriohepatic dysplasia (Alagille syndrome): extreme variability among affected family members

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12 December 2020

Conservation of the paired domain in metazoans and its structure in three isolated human genes

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12 December 2020

Alagille syndrome with de Novo del(20) (p 11.2)

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12 December 2020

undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1

1 reference

12 December 2020

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

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12 December 2020

Deleted chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes

1 reference

12 December 2020

Mapping of microsatellite markers in the Alagille region and screening of microdeletions by genotyping 23 patients

1 reference

12 December 2020

Screening of microdeletions of chromosome 20 in patients with Alagille syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00209488

1 reference

15 August 2017

1 reference