Is it possible to make a clinical diagnosis of the fragile X syndrome in a boy? (Q35602538)

9 August 2017

Is it possible to make a clinical diagnosis of the fragile X syndrome in a boy? (English)

1 reference

9 August 2017

1 reference

Thake A

1

1 reference

9 August 2017

Todd J

series ordinal

2

1 reference

9 August 2017

Bundey S

series ordinal

3

1 reference

9 August 2017

Webb T

series ordinal

4

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 November 1985

1 reference

Archives of Disease in Childhood

9 August 2017

1 reference

9 August 2017

60

1 reference

9 August 2017

11

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9 August 2017

1001-1007

1 reference

The assessment of growth and development in children

9 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Growth of the skull in young children. I. Standards of head circumference

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

X-linked mental retardation with the fragile X. A study of 15 families

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

X-linked mental retardation, macro-orchidism, and the Xq27 fragile site

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Autism and the fragile X syndrome.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Screening of mentally retarded males for macro-orchidism and the fragile X chromosome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Testicular size: assessment and clinical importance

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

12 July 2018

A marker X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

A Growth Chart for Premature and Other Infants

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

X-linked mental retardation.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

VI. Somatic pubertal development

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Familial X-linked mental retardation with an X chromosome abnormality

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

X-linked mental retardation with macro-orchidism and marker X chromosomes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Fragile X-linked mental retardation: the Martin-Bell syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

The fragile X syndrome. A study of 83 families.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

Head circumference from birth to eighteen years. Practical composite international and interracial graphs

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777630

A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome

15 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4073931

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Lengths of the growing foot

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4073931

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ADC.60.11.1001

1 reference

9 August 2017

1 reference

9 August 2017

1 reference