Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q33671267)
Watch
English
A case of deletion 2q35----qter and a peculiar phenotype
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
title
A case of deletion 2q35----qter and a peculiar phenotype
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
author name string
Sánchez JM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
Pantano AM
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
language of work or name
English
0 references
publication date
1 April 1984
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
volume
21
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
page(s)
147-149
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
cites work
Craniosynostosis, midfacial hypoplasia, and foot abnormalities: An autosomal dominant phenotype in a large Amish kindred
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=1049247
retrieved
21 June 2018
Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31).
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=1049247
retrieved
30 October 2018
A rapid banding technique for human chromosomes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6716416
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A girl with a deletion (2) (q34q36): cytogenetic and clinical observations (author's transl)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6716416
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Partial deletion of chromosome 2 mimicking a phenotype of trisomy 18: case report with autopsy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6716416
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.21.2.147
0 references
PMCID
1049247
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 2017
PubMed ID
6716416
1 reference
stated in
Europe PubMed Central
PubMed ID
6716416
retrieved
28 July 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
