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A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34.
scientific article
A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
case report
0 references
title
A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
main subject
microcephaly
0 references
primary autosomal recessive microcephaly
0 references
author
Andrew Jackson
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Nicholas Lench
series ordinal
9
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
C Geoffrey Woods
series ordinal
10
object named as
Woods CG
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
author name string
Moynihan L
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Roberts E
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Karbani G
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Lewis I
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Corry P
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Turner G
series ordinal
7
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Mueller RF
series ordinal
8
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
language of work or name
English
0 references
publication date
1 February 2000
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
volume
66
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
page(s)
724-727
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
cites work
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
24 March 2017
C3G, a guanine nucleotide-releasing protein expressed ubiquitously, binds to the Src homology 3 domains of CRK and GRB2/ASH proteins
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
24 March 2017
Faster sequential genetic linkage computations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
7 April 2017
A physical map of 30,000 human genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
27 September 2017
Mapping of the human C3G gene coding a guanine nucleotide releasing protein for Ras family to 9q34.3 by fluorescence in situ hybridization.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
27 September 2017
Hox gene products modulate the DNA binding activity of Pbx1 and Pbx2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
27 September 2017
Familial microcephaly with normal intelligence in a patient with acute lymphoblastic leukemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
27 September 2017
The genetics and sub-classification of microcephaly
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
30 May 2018
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
30 May 2018
Autosomal recessive nonsyndromal microcephaly with normal intelligence
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
30 May 2018
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected child
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
30 May 2018
Segregation frequency in microcephaly
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
30 May 2018
The Pbx family of proteins is strongly upregulated by a post-transcriptional mechanism during retinoic acid-induced differentiation of P19 embryonal carcinoma cells.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
29 November 2018
Avoiding recomputation in linkage analysis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288125
retrieved
29 November 2018
Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10677332
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1086/302777
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
PMC publication ID
1288125
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
PubMed publication ID
10677332
1 reference
stated in
Europe PubMed Central
PMC publication ID
1288125
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677332%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
ResearchGate publication ID
12638763
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