(Q35602686)

9 August 2017

title

Chromosome abnormalities in pupils attending ESN/M schools (English)

1 reference

9 August 2017

Lamont MA

1

1 reference

9 August 2017

Dennis NR

series ordinal

2

1 reference

9 August 2017

Seabright M

series ordinal

3

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 March 1986

1 reference

Archives of Disease in Childhood

9 August 2017

published in

1 reference

9 August 2017

volume

61

1 reference

9 August 2017

issue

3

1 reference

9 August 2017

page(s)

223-226

1 reference

Etiological study of mental retardation in Budapest, Hungary.

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Gonadal dysgenesis in a patient with an X;3 translocation: case report and review

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Mild mental retardation in Swedish school children. II. Etiologic and pathogenetic aspects.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Fragile site X chromosomes and X-linked mental retardation in severely retarded boys in a northern Swedish county. A prevalence study.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Detection of the fragile X chromosome and other fragile sites.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

A cytogenetic survey of 11,680 newborn infants

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Severe Mental Retardation in a Swedish County – II. Etiologic and Pathogenetic Aspects of Children Born 1959–1970

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Learning disorders and sex chromosome aberrations.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Klinefelter's syndrome in adolescence.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Marker X-associated mental retardation. A study of 150 retarded males.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Clinical assessment of 4500 developmentally delayed individuals

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777694

Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2421647

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A rapid banding technique for human chromosomes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2421647

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ADC.61.3.223

1 reference

9 August 2017

1 reference

9 August 2017

1 reference