(Q42654681)

4 November 2017

Inv dup (15) with mental retardation but few dysmorphic features (English)

1 reference

4 November 2017

Gilmore DH

1

1 reference

4 November 2017

Boyd E

2

1 reference

4 November 2017

McClure JP

3

1 reference

4 November 2017

Batstone P

4

1 reference

4 November 2017

Connor JM

5

1 reference

4 November 2017

language of work or name

English

0 references

publication date

1 June 1984

1 reference

Journal of Medical Genetics

4 November 2017

1 reference

4 November 2017

21

1 reference

4 November 2017

3

1 reference

4 November 2017

221-223

1 reference

Extra dicentric 15 pter leads to q21/22 chromosomes in five unrelated patients with a distinct syndrome of progressive psychomotor retardation, seizures, hyper-reactivity and dermatoglyphic abnormalities.

4 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049272

Partial trisomy of chromosome 15.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049272

Partial trisomy 15 in a young girl

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049272

Cytogenetic and clinical studies in five cases of inv dup(15)

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049272

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049272

Partial trisomy 15 and intractable seizures

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049272

A G-like trisomy with a major 15 proximal supernumerary component derived from a D/E balanced maternal interchange

27 May 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6748020

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A case of extra small acrocentric bisatellited chromosome in a non mongoloid child

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6748020

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

An extra idic(15p)(q11) chromosome in Prader-Willi syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6748020

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

4 November 2017

PubMed publication ID

6748020

1 reference