(Q24672141)

English

Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

0 references

Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome (English)

0 references

holoprosencephaly

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

M Muenke

1

0 references

L J Bone

2

0 references

H F Mitchell

3

0 references

I Hart

4

0 references

K Walton

5

0 references

K Hall-Johnson

6

0 references

E F Ippel

7

0 references

J Dietz-Band

8

0 references

K Kvaløy

9

0 references

C M Fan

10

0 references

language of work or name

0 references

publication date

November 1995

0 references

American Journal of Human Genetics

0 references

57

0 references

5

0 references

1074-9

0 references

Physical mapping of the holoprosencephaly critical region in 18p11.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

7 April 2017

A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

7 April 2017

Down syndrome phenotypes: the consequences of chromosomal imbalance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

A transcript map of the Down syndrome critical region on chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

The Drosophila single-minded gene encodes a helix-loop-helix protein that acts as a master regulator of CNS midline development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

Drosophila single-minded gene and the molecular genetics of CNS midline development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

Continuum of overlapping clones spanning the entire human chromosome 21q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

Isolation of chromosome 21-specific yeast artificial chromosomes from a total human genome library

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 September 2017

Physical mapping of the holoprosencephaly critical region on chromosome 7q36.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

30 May 2018

A male infant with holoprosencephaly, associated with ring chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

30 May 2018

The Drosophila single-minded gene encodes a nuclear protein with sequence similarity to the per gene product

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

30 May 2018

Partial physical map of human chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

30 May 2018

Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

30 May 2018

The single-minded gene of Drosophila is required for the expression of genes important for the development of CNS midline cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

30 May 2018

Sublocalization on chromosome 21 of human interferon-alpha receptor gene and the gene for an interferon-gamma response protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

30 May 2018

Report of the Fifth International Workshop on Human Chromosome 21 Mapping 1994

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801356

28 November 2018

Irradiation-reduced human chromosome 21 hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/7485157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the fourth international workshop on human chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/7485157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the squalene synthase gene (FDFT1) to human chromosome 8p22-p23.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7485157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positional cloning moves from perditional to traditional

1 reference

https://pubmed.ncbi.nlm.nih.gov/7485157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991

1 reference

https://pubmed.ncbi.nlm.nih.gov/7485157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

0 references

PubMed publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24672141&oldid=1604320008"