(Q69751001)

English

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

scientific article published on 01 October 1989

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2793167%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

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

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2793167%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

Alagille syndrome

1 reference

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author name string

S Schnittger

1

1 reference

Europe PubMed Central

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5 October 2019

C Höfers

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2793167%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

P Heidemann

3

1 reference

Europe PubMed Central

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5 October 2019

F Beermann

4

1 reference

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5 October 2019

I Hansmann

5

1 reference

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5 October 2019

publication date

1 October 1989

1 reference

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5 October 2019

1 reference

Europe PubMed Central

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5 October 2019

83

1 reference

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5 October 2019

3

1 reference

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5 October 2019

239-244

1 reference

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5 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00285164

0 references

Deletion of the short arm of chromosome 20

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A partial short arm deletion of chromosome 20:46, XY, del(20)(p11)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of the short arms of chromosome 20

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term prognosis for infants with intrahepatic cholestasis and patent extrahepatic biliary tract

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Del(20p) with manifestations of arteriohepatic dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Arteriohepatic dysplasia: phenotypic features and family studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary cholestasis combined with peripheral pulmonary stenosis and other anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of the short arm of chromosome 20

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cholestatic jaundice in infancy. The importance of familial and genetic factors in aetiology and prognosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid banding technique for routine use in human and comparative cytogenetics.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high resolution in situ hybridization technique for the direct visualization of labeled G-banded early metaphase and prophase chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monosomy 20p due to a de novo del(20)(p12.2). Clinical and radiological delineation of the syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The primary structure of human secretogranin I (chromogranin B): comparison with chromogranin A reveals homologous terminal domains and a large intervening variable region

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Application of DNA analysis to mapping the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction fragment length polymorphisms at the human parathyroid hormone gene locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cytogenetics: toward dissection of the contiguous gene syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of a human prion protein cDNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paucity of interlobular bile ducts getting to know it better

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the human and mouse prion protein genes to homologous chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The map of chromosome 20.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Arteriohepatic dysplasia (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene encoding human growth hormone-releasing factor precursor: structure, sequence, and chromosomal assignment

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial deletion of the short arm of chromosome 20: 46,XX,del(20)(p11)/46,XX mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contiguous gene syndromes: a component of recognizable syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and sequence analysis of cDNA for the precursor of human growth hormone-releasing factor, somatocrinin

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allocation of a transgenic c-myc integration site to mouse chromosome 8B3-C1

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple congenital malformations in a boy with a chromosome abnormality of the group F (46-XY, 20-P), the son of a clinically healthy subject with an analogous chromosome malformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2793167

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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