(Q70613513)

English

Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism

scientific article published on 01 March 1993

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454295%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454295%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

author name string

H Traupe

1

1 reference

Europe PubMed Central

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12 October 2019

U Vetter

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454295%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

R Happle

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454295%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

L W Fisher

4

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Europe PubMed Central

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12 October 2019

F P Cremers

5

1 reference

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12 October 2019

S J Landy

6

1 reference

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12 October 2019

R Pankau

7

1 reference

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12 October 2019

H H Ropers

8

1 reference

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12 October 2019

publication date

1 March 1993

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12 October 2019

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454295%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

91

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12 October 2019

1

1 reference

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12 October 2019

89-90

1 reference

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12 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00230233

0 references

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked dominant Conradi-Hünermann syndrome presenting as congenital erythroderma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deduced protein sequence of bone small proteoglycan I (biglycan) shows homology with proteoglycan II (decorin) and several nonconnective tissue proteins in a variety of species

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physical map of human Xq27-qter: localizing the region of the fragile X mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human biglycan gene. Putative promoter, intron-exon junctions, and chromosomal localization

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homologous genes for X-linked chondrodysplasia punctata in man and mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked dominant chondrodysplasia punctata. Review of literature and report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression and localization of the two small proteoglycans biglycan and decorin in developing human skeletal and non-skeletal tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of the mouse X chromosome in the region homologous to human Xq27–Xq28

1 reference

https://pubmed.ncbi.nlm.nih.gov/8454295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00230233

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454295%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454295%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

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