(Q24600272)

12

object named as

Randi Hagerman

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author name string

Nicole Tartaglia

1

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Shanlee Davis

2

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Alison Hench

3

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Sheela Nimishakavi

4

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Renee Beauregard

5

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Ann Reynolds

6

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Laura Fenton

7

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Lindsey Albrecht

8

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Judith Ross

9

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Robin Hansen

American Journal of Medical Genetics Part A

11

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language of work or name

English

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publication date

15 June 2008

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published in

1 reference

Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY

volume

146A

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issue

12

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page(s)

1509-22

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cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Parental origin of the extra chromosomes in polysomy X

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Sex chromosome tetrasomy and pentasomy

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Analyses of data on rates of cytogenetic disorders in live births

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Male pubertal development and the role of androgen therapy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Essential tremor: emerging views of a common disorder

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Cancer incidence and mortality in men with Klinefelter syndrome: a cohort study

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

X-chromosome inactivation patterns and androgen receptor functionality influence phenotype and social characteristics as well as pharmacogenetics of testosterone therapy in Klinefelter patients

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

KLINEFELTER'S SYNDROME DUE TO XXYY CHROMOSOME ANOMALY

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

THE XXYY VARIANT OF KLINEFELTER'S SYNDROME

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

A probable XXYY sex determining mechanism in a mentally defective male with Klinefelter's syndrome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

XXYY syndrome discovered on routine physical examination

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Dermatoglyphics in XXYY Klinefelter's syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Sex chromosome aberrations and speech development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Testosterone treatment of an XXYY male presenting with aggression: a case report

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Klinefelter syndrome and neurological disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

A male patient with 48,XXYY syndrome: importance of distinction from Klinefelter's syndrome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Improvement of peripheral neuropathy by testosterone in a patient with 48,XXYY syndrome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

An XXYY male with schizophrenia.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

XYY syndrome, and XYY-XXYY mosaicism also showing features of Klinefelter's syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Variation in the decision to terminate pregnancy in the setting of fetal aneuploidy

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Essential tremor among children

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

A CASE OF A MENTALLY DEFECTIVE MALE WITH XXYY SEX CHROMOSOME CONSTITUTION.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Clinical findings and phenotype in a toddler with 48,XXYY syndrome.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Congenital heart disease in the 48,XXYY syndrome

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Mental illness, epilepsy and hypothyroidism in XXYY syndrome.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

Bone abnormalities and XXYY.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056496

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

28 November 2018

1 reference

12 December 2020

The 48, XXYY syndrome

1 reference

12 December 2020

A special form of Klinefelter's syndrome: mosaic with doubling of the Y chromosome (2 X-2 Y form)

1 reference

12 December 2020

TWO CASES OF (PREPUBERTAL) KLINEFELTER'S SYNDROME WITH XXYY SEX CHROMOSOMES

1 reference

12 December 2020

Androgen replacement in a 48, XXYY-male patient

1 reference

12 December 2020

KLINEFELTER'S SYNDROME WITH THE XXYY SEX CHROMOSOME COMPLEX. WITH PARTICULAR REFERENCE TO PREPUBERTAL DIAGNOSIS

1 reference

12 December 2020

Two cases of 48,XXYY: with discussion on the behaviour of prepubertal and postpubertal patients

1 reference

12 December 2020

1 reference

12 December 2020

The XXYY chromosome constitution. Deoxyribonucleic acid replication and the Xg blood group

1 reference

12 December 2020

AN XXYY VARIANT OF THE KLINEFELTER SYNDROME IN A PREPUBERTAL BODY

1 reference

12 December 2020

Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients

1 reference

12 December 2020

Combined Klinefelter-Down syndrome or XXYY syndrome?

1 reference

12 December 2020

Colobomas of the iris and choroid and high signal intensity cerebral foci on T2-weighted magnetic resonance images in Klinefelter's syndrome

1 reference

12 December 2020

Expression of SHOX in human fetal and childhood growth plate

1 reference

12 December 2020

[48,XXYY syndrome in a boy with essential tremor. Comparison with 120 cases from the literature]

1 reference

12 December 2020

STUDIES ON A BOY WITH XXYY CHROMOSOME CONSTITUTION

1 reference

12 December 2020

Users' guides to the medical literature: XXIV. How to use an article on the clinical manifestations of disease. Evidence-Based Medicine Working Group

1 reference

12 December 2020

A case of 48,XXYY Klinefelter's syndrome with incurable skin ulcer

1 reference

12 December 2020

The 48,XXYY syndrome: a case detected by maternal serum alpha-fetoprotein screening

1 reference

12 December 2020

48,XXYY syndrome associated with acromegaloidism

1 reference

12 December 2020

Case Studies of Three “XXYY” Children

1 reference

12 December 2020

YY chromosomes and Klinefelter's syndrome

1 reference

12 December 2020

Two 48,XXYY patients: clinical, cytogenetic and molecular aspects

1 reference

12 December 2020

Efficacy of unilateral deep brain stimulation of the thalamic ventralis intermedius nucleus in a patient with bipolar disorder associated with Klinefelter syndrome and essential tremor. Case report

1 reference

12 December 2020

Klinefelter's syndrome and essential tremor

1 reference

12 December 2020

THE "DOUBLE MALE": A NEW CHROMOSOME CONSTITUTION IN KLINEFELTER'S SYNDROME

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FAJMG.A.32366

7 January 2021