(Q72345845)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

Positional cloning moves from perditional to traditional (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1

Collins FS

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

publication date

1 April 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

volume

9

1 reference

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26 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

page(s)

347-350

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng0495-347

26 October 2019

exact match

0 references

cites work

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Positional cloning: let's not call it reverse anymore

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

The rise and fall of positional cloning?

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Trinucleotide repeat expansions and human genetic disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Location on chromosome 15 of the gene defect causing Marfan syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

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%2FNG0495-347

7 January 2021

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Mutations of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4.

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Genetic dissection of complex traits

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

A genome-wide search for human type 1 diabetes susceptibility genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Light-generated oligonucleotide arrays for rapid DNA sequence analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-347

7 January 2021

Identifiers

DOI

10.1038/NG0495-347

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference