Partial monosomy 8p with minimal dysmorphic signs (Q33597710)

28 July 2017

title

Partial monosomy 8p with minimal dysmorphic signs (English)

1 reference

28 July 2017

Blennow E

1

1 reference

28 July 2017

Bröndum-Nielsen K

series ordinal

2

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 May 1990

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

27

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28 July 2017

issue

5

1 reference

28 July 2017

page(s)

327-329

1 reference

Monosomy 8p: an easily overlooked syndrome.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017085

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017085

Partial deletion of the short arm of chromosome 8

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017085

Small structural changes of chromosome 8. Two cases with evidence for deletion

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017085

New chromosomal malformation syndromes. I. Partial monosomy 8p. An attempt to establish a new chromosome deletion syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017085

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017085

Partial deletion of the short arm of chromosome 8

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017085

21 June 2018

Partial 8p- syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017085

A new chromosome deletion syndrome. Report of a patient with a 46, XY,8p‐ chromosome constitution

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2352261

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A case of deletion of short arm of chromosome 8

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2352261

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Report of the committee on the genetic constitution of chromosomes 2, 3, 4, 5, 7, 8, 10, 11, and 12

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2352261

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.27.5.327

1 reference

28 July 2017

1 reference

28 July 2017

1 reference