(Q34769804)

PubMed publication ID

18410780

4 August 2017

title

Effect of ascertainment and genetic features on the phenotype of Klinefelter syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

3

Najiba Lahlou

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

author name string

Martha P D Zeger

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

Purita Ramos

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

Karen Kowal

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

Carole Samango-Sprouse

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

Judith L Ross

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

language of work or name

English

0 references

publication date

21 December 2007

1 reference

PubMed publication ID

18410780

The Journal of Pediatrics

4 August 2017

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

volume

152

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

page(s)

716-722

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

Serum inhibin B levels during male childhood and puberty

12 May 2020

cites work

1 reference

12 December 2020

Mental development in polysomy X Klinefelter syndrome (47,XXY; 48,XXXY): effects of incomplete X inactivation

1 reference

12 December 2020

Diagnosis and management of the adolescent boy with Klinefelter syndrome.

1 reference

12 December 2020

Prevalence of obesity, diabetes, and obesity-related health risk factors, 2001

1 reference

12 December 2020

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

1 reference

12 December 2020

Longitudinal studies of inhibin B levels in boys and young adults with Klinefelter syndrome

1 reference

12 December 2020

Chromatin test in Klinefelter's syndrome

1 reference

12 December 2020

Klinefelter syndrome: expanding the phenotype and identifying new research directions

1 reference

12 December 2020

Inhibin B and anti-Müllerian hormone, but not testosterone levels, are normal in infants with nonmosaic Klinefelter syndrome

1 reference

12 December 2020

Klinefelter syndrome in adolescence: onset of puberty is associated with accelerated germ cell depletion

1 reference

12 December 2020

Ascertainment bias in Turner syndrome: new insights from girls who were diagnosed incidentally in prenatal life

1 reference

12 December 2020

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

1 reference

12 December 2020

Early androgen deficiency in infants and young boys with 47,XXY Klinefelter syndrome

1 reference

12 December 2020

Natural history of seminiferous tubule degeneration in Klinefelter syndrome

1 reference

12 December 2020

Are Adolescent Boys with Klinefelter Syndrome Androgen Deficient? A Longitudinal Study of Finnish 47,XXY Boys

1 reference

12 December 2020

Activating mutations in the luteinizing hormone receptor gene: a human model of non-follicle-stimulating hormone-dependent inhibin production and germ cell maturation

1 reference

12 December 2020

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

1 reference

12 December 2020

Growth, development, and behavioral outcome from mid-adolescence to adulthood in subjects with chromosome aneuploidy: the Toronto Study

1 reference

12 December 2020

Summary of clinical findings in children and young adults with sex chromosome anomalies

1 reference

12 December 2020

The parental origin of 47,XXY males

1 reference

12 December 2020

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

1 reference

12 December 2020

Pituitary-gonadal function in Klinefelter syndrome before and during puberty

1 reference

12 December 2020

Physical growth: National Center for Health Statistics percentiles

1 reference

12 December 2020

The XXY (Klinefelter's) syndrome in childhood: Detection and treatment

1 reference

12 December 2020

Summary of clinical findings of children with 47,XXY, 47,XYY, and 47,XXX karyotypes

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1016/J.JPEDS.2007.10.019

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

release_ik5he2l5ufddxk6fplemmb3i4u

12 May 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ik5he2l5ufddxk6fplemmb3i4u

24 November 2022

mapped directly with Wikidata item

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6728163&resulttype=core&format=json

12 May 2020

PubMed publication ID

18410780

1 reference