Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q42041694)
Watch
English
Molecular cytogenetics: toward dissection of the contiguous gene syndromes
scientific article published on November 1988
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
title
Molecular cytogenetics: toward dissection of the contiguous gene syndromes
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
main subject
cytogenetics
1 reference
based on heuristic
inferred from title
author name string
Emanuel BS
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
language of work or name
English
0 references
publication date
1 November 1988
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
volume
43
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
page(s)
575-578
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
issue
5
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
cites work
Segmental aneuploidy and the genetic gross structure of the Drosophila genome
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=1715556
retrieved
5 June 2018
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
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=1715556
retrieved
5 June 2018
Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients.
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=1715556
retrieved
5 June 2018
Chromosome abnormalities in pediatric brain tumors.
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=1715556
retrieved
5 June 2018
Cytogenetic findings in a prospective series of patients with DiGeorge anomaly
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=1715556
retrieved
5 June 2018
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome
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=1715556
retrieved
5 June 2018
Contiguous gene syndromes: a component of recognizable syndromes
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=1715556
retrieved
5 June 2018
Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.
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=1715556
retrieved
5 June 2018
Reverse genetics and human disease
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=1715556
retrieved
5 June 2018
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci
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=1715556
retrieved
17 August 2018
Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3189328
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1715556
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
PubMed ID
3189328
1 reference
stated in
Europe PubMed Central
PMCID
1715556
retrieved
15 October 2017
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
