(Q34811120)

4 August 2017

1 reference

title

Genes and translocations involved in POF. (English)

1 reference

4 August 2017

1

David Schlessinger

0 references

Laura Crisponi

3

object named as

Laura Crisponi

0 references

Giuseppe Pilia

7

object named as

Giuseppe Pilia

1 reference

4 August 2017

Luisa Herrera

2

1 reference

4 August 2017

Steven Mumm

4

1 reference

4 August 2017

Antonio Percesepe

5

1 reference

4 August 2017

Massimo Pellegrini

6

1 reference

4 August 2017

Antonino Forabosco

8

1 reference

4 August 2017

1 August 2002

1 reference

American Journal of Medical Genetics Part A

4 August 2017

1 reference

4 August 2017

111

1 reference

4 August 2017

3

1 reference

4 August 2017

328-333

1 reference

Premature ovarian failure: an update.

4 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

A quantitative and cytological study of germ cells in human ovaries

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Follicle dynamics during ovarian ageing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Morphometric study of the human neonatal ovary.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Tissue-specific Bcl-2 protein partners in apoptosis: An ovarian paradigm

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Report of the committee on the genetic constitution of chromosome 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

The X bivalent in fetal bovine oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

X chromosome imprinting and inactivation in the early mammalian embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

The role of X-chromosome inactivation during spermatogenesis (Drosophila-allocycly-chromosome evolution-male sterility-dosage compensation).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Unpaired chromosomes at meiosis: cause or effect of gametogenic insufficiency?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Oocyte apoptosis is suppressed by disruption of the acid sphingomyelinase gene or by sphingosine-1-phosphate therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Studies of FRAXA and FRAXE in women with premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Microdeletions in FMR2 may be a significant cause of premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Brief historical note: The concept of “gonadal dysgenesis”

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Physical mapping of DNA markers in the q13-q22 region of the human X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

4.5-Mb YAC STS contig at 50-kb resolution, spanning Xq25 deletions in two patients with lymphoproliferative syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Clinical review 6: Diagnosis and management of delayed puberty

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Ovarian differentiation and gonadal failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Choroideremia associated with an X-autosomal translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

The possible role of meiotic pairing anomalies in the atresia of human fetal oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Evidence for a secular trend in age of menarche.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

Turner syndrome: the case of the missing sex chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10565

21 January 2018

Identifiers

DOI

10.1002/AJMG.10565

1 reference

4 August 2017

1 reference