(Q33876064)

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An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20014371%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20014371%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

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based on heuristic

inferred from title

4

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15 January 2020

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Judith L Ross

1

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15 January 2020

Martha P D Zeger

2

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15 January 2020

Harvey Kushner

3

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15 January 2020

David P Roeltgen

5

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Europe PubMed Central

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15 January 2020

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1 January 2009

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Europe PubMed Central

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15 January 2020

Developmental Disabilities Research Reviews

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20014371%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

15

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20014371%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

4

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Europe PubMed Central

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15 January 2020

309-317

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20014371%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Abnormal sex chromosome constitution and longitudinal growth: serum levels of insulin-like growth factor (IGF)-I, IGF binding protein-3, luteinizing hormone, and testosterone in 109 males with 47,XXY, 47,XYY, or sex-determining region of the Y chrom

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Abnormalities of sex chromosome constitution in newborn babies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Long-term outcome in children of sex chromosome abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Volumetric magnetic resonance imaging study of the brain in subjects with sex chromosome aneuploidies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

The psychoeducational profile of boys with Klinefelter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Intelligence and achievement in children with extra X aneuploidy: a longitudinal perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Neuropsychological impairment in 42 adolescents with sex chromosome abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

The pseudoautosomal regions of the human sex chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Prenatal testosterone levels in XXY and XYY males

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Mental development of unselected children with sex chromosome abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Speech and learning disorders in children with sex chromosome abnormalities.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

The development of four unselected 47,XYY boys.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

A psychological study of the personalities of XYY- and XXY-men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Variations in pattern of pubertal changes in girls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Testosterone excretion rates in normal males and males with an XYY complement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Psychological Studies of Ten Patients with the XYY Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Assessing children's copy productions of the Rey-Osterrieth Complex Figure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

X chromosome abnormalities and cognitive development: implications for understanding normal human development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Edinburgh study of growth and development of children with sex chromosome abnormalities. III.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Sex chromosomal aneuploidy: prospective and longitudinal studies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Growth and development from early to midadolescence of children with X and Y chromosome aneuploidy: the Toronto Study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Oral and written language abilities of XXY boys: implications for anticipatory guidance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Verbal deficits in Klinefelter (XXY) adults living in the community

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Cognitive and behavioral factors in the learning disabilities of 47,XXY and 47,XYY boys

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Sex chromosome aneuploidy: the Denver Prospective Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Growth during puberty in the XYY boy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

The growth and development of six XYY children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Physical growth: National Center for Health Statistics percentiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

Testicular function in XYY men

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

5 July 2018

X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

29 October 2018

Cognitive and motor development during childhood in boys with Klinefelter syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

29 October 2018

Degree of handedness and cerebral dominance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

29 October 2018

Stimulant medication in 47,XYY syndrome: a report of two cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

29 October 2018

The XYY syndrome: a follow-up study on 38 boys

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2876236

29 October 2018

Physical and psychologic parameters in children with sex chromosome anomalies: further follow-up from the Winnipeg Cytogenetic Study of 14,069 newborn infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prospective study of development of children with sex chromosome anomalies: New Haven Study IV. Adolescence

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Summary overview of behavioural development in individuals with neonatally identified X and Y aneuploidy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gross and fine motor development in 47,XXY and 47,XYY males

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The XYY condition in childhood: clinical observation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma testosterone levels in males with the 47,XYY karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetics, hormones and behavior disability: comparison of XYY and XXY syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Edinburgh study of growth and development of children with sex chromosome abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A group-test for assessing hand- and eye-dominance

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of sex chromosome abnormalities: the 8-year experience of a single medical center

1 reference

https://pubmed.ncbi.nlm.nih.gov/20014371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurobehavioral phenotype of Klinefelter syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDDRR.85

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/DDRR.85

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20014371%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20014371%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20014371%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

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