(Q33586421)

28 July 2017

title

Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome (English)

1 reference

human chromosomes 6-12 and X

28 July 2017

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1121016

23 August 2022

1 reference

https://api.crossref.org/works/10.1136/JMG.12.1.105

2 October 2023

author name string

N. C. Magnelli

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1121016

23 August 2022

E. Therman

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1121016

23 August 2022

publication date

1 March 1975

1 reference

full work available at URL

28 July 2017

language of work or name

English

0 references

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1121016/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1121016

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1121016/pdf/?tool=EBI

23 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1121016

http://jmg.bmjjournals.com/cgi/content/abstract/12/1/105

23 August 2022

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1121016

https://europepmc.org/articles/PMC1013240

23 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1121016

https://europepmc.org/articles/PMC1013240?pdf=render

23 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1121016

https://jmg.bmj.com/content/jmedgenet/12/1/105.full.pdf

23 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1121016

https://syndication.highwire.org/content/doi/10.1136/jmg.12.1.105

2 October 2023

1 reference

https://api.crossref.org/works/10.1136/JMG.12.1.105

Journal of Medical Genetics

2 October 2023

published in

1 reference

28 July 2017

volume

12

1 reference

28 July 2017

issue

1

1 reference

28 July 2017

page(s)

105-108

1 reference

FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA

28 July 2017

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013240

Cytological studies on a human ring chromosome

21 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013240

LONGITUDINAL DIFFERENTIATION OF CHROMOSOMES AND THE POSSIBILITY OF INTERSTITIAL TELOMERES

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1121016

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Partial monosomy of a C group chromosome (Cp-)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1121016

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Cytogenetics in mentally defective children with anomalies: a controlled study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1121016

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.12.1.105

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1121016

23 August 2022

1 reference

28 July 2017

1 reference