(Q81470868)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16283387%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions (English)

1 reference

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9 January 2020

1

1 reference

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9 January 2020

author name string

S Youings

2

1 reference

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9 January 2020

T Costa

3

1 reference

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9 January 2020

P A Jacobs

4

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9 January 2020

N S Thomas

5

1 reference

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9 January 2020

publication date

8 November 2005

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9 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16283387%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

118

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9 January 2020

issue

5

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9 January 2020

page(s)

640-651

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The critical region on the human Xq.

9 January 2020

cites work

1 reference

12 December 2020

Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients

1 reference

12 December 2020

Ullrich-Turner syndrome: seven pregnancies in an apparent 45,X woman

1 reference

12 December 2020

Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene

1 reference

12 December 2020

Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?

1 reference

12 December 2020

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

Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location

1 reference

12 December 2020

Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height

1 reference

12 December 2020

Atypical phenotype in a female with a large Xp deletion

1 reference

12 December 2020

Molecular analysis of genes on Xp controlling Turner syndrome and premature ovarian failure (POF).

1 reference

12 December 2020

A study of females with deletions of the short arm of the X chromosome

1 reference

12 December 2020

Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features

1 reference

12 December 2020

Height correlations between parents and mature offspring in normal subjects and in subjects with Turner's and Klinefelter's and other syndromes

1 reference

12 December 2020

Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features

1 reference

12 December 2020

Balanced structural changes involving the human X: Effect on sexual phenotype

1 reference

12 December 2020

Xp deletions associated with autism in three females

1 reference

12 December 2020

The Turner syndrome-associated neurocognitive phenotype maps to distal Xp

1 reference

12 December 2020

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

1 reference

12 December 2020

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

1 reference

12 December 2020

The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism

1 reference

12 December 2020

Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.

1 reference

12 December 2020

Deletion of the short arm of the X chromosome: a hereditary form of Turner syndrome

1 reference

12 December 2020

X chromosome constitution and the human female phenotype

1 reference

12 December 2020

An excess of chromosome 1 breakpoints in male infertility

1 reference

12 December 2020

Molecular and cytogenetic analysis of familial Xp deletions

1 reference

12 December 2020

Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: implications for the development of Turner syndrome

1 reference

12 December 2020