A common region of 10p deleted in DiGeorge and velocardiofacial syndromes (Q57251931)

10

0 references

Thomas Meitinger

object named as

Thomas Meitinger

7

0 references

Judith A Goodship

9

object named as

Judith Goodship

0 references

author name string

Sara C.M. Daw

1

0 references

Catherine Taylor

2

0 references

Kathy Call

4

0 references

Jen-i Mao

5

0 references

Simone Schuffenhauer

6

0 references

Tony Lipson

https://scigraph.springernature.com/pub.10.1038/ng0896-458

8

0 references

language of work or name

English

0 references

publication date

August 1996

0 references

published in

Nature Genetics

0 references

volume

13

0 references

page(s)

458-460

0 references

issue

4

0 references

exact match

0 references

cites work

Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

DiGeorge syndrome: part of CATCH 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

An STS-based map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

Assignment of the gene encoding the beta-subunit of the human fibronectin receptor (beta-FNR) to chromosome 10p11.2

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

Fine genetic mapping of the proximal part of mouse chromosome 2 excludes Pax-8 as a candidate gene for Danforth's short tail (Sd)

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

Yeast artificial chromosome libraries containing large inserts from mouse and human DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

An optimized Alu-PCR primer pair for human-specific amplification of YACs and somatic cell hybrids

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-458

7 January 2021