(Q35167177)

6 August 2017

1 reference

title

Contemporary issues in primary amenorrhea (English)

1 reference

6 August 2017

0 references

Lorna S Timmreck

1

1 reference

PubMed ID

12836721

6 August 2017

Richard H Reindollar

series ordinal

2

1 reference

6 August 2017

1 June 2003

1 reference

Obstetrics and Gynecology Clinics of North America

6 August 2017

1 reference

6 August 2017

30

1 reference

6 August 2017

2

1 reference

6 August 2017

287-302

1 reference

Delayed sexual development: a study of 252 patients

6 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

A cytogenetic and endocrinologic study of a set of monozygotic isokaryotic 45,X/46,XY twins discordant for phenotypic sex: mosaicism versus chimerism

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Further delineation of aortic dilation, dissection, and rupture in patients with Turner syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Twins Discordant for 46,XX Gonadal Dysgenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Ovarian differentiation and gonadal failure

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Mapping of the POF1 locus and identification of putative genes for premature ovarian failure

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Premature ovarian failure in the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Molecular genetic, biochemical, and clinical implications of gonadotropin receptor mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

A Novel mutation in the FSH receptor inhibiting signal transduction and causing primary ovarian failure.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Genetic analysis of the cytochrome P-450c17alpha (CYP17) and aldosterone synthase (CYP11B2) in Japanese patients with 17alpha-hydroxylase deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Evidence that the SRY protein is encoded by a single exon on the human Y chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Paternal somatic and germ-line mosaicism for a sex-determining region on Y (SRY) missense mutation leading to recurrent 46,XY sex reversal

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Camptomelic dwarfism associated with XY-gonadal dysgenesis and chromosome anomalies

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Mutation analysis of the gonadotropin-releasing hormone receptor gene in idiopathic hypogonadotropic hypogonadism

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Inherited disorders of GnRH and gonadotropin receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

The molecular basis of human hypogonadotropic hypogonadism

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Hypogonadotropic hypogonadism in a female caused by an X-linked recessive mutation in the DAX1 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone beta-subunit gene

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Canalization failure of the müllerian tract

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Congenital absence of the uterus and vagina is not commonly transmitted as a dominant genetic trait: outcomes of surrogate pregnancies.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Analysis of cystic fibrosis transmembrane conductance regulator gene mutations in patients with congenital absence of the uterus and vagina.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Role for anti-Müllerian hormone in congenital absence of the uterus and vagina

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Further evidence that the WT1 gene does not have a role in the development of the derivatives of the müllerian duct.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Familial Syndrome of Streak Gonads and Normal Male Karyotype in Five Phenotypic Females

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

The molecular basis of androgen insensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Increased bone mass as a result of estrogen therapy in a man with aromatase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

Estrogen deficiency is a potential cause for osteopenia in adult male patients with Noonan's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8545%2803%2900027-5

7 January 2021

10.1016/S0889-8545(03)00027-5

Identifiers

DOI

1 reference

6 August 2017

1 reference

PubMed ID

12836721