(Q52140917)

23 April 2018

title

A fork in the road to fertility. (English)

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23 April 2018

author

Andrew R. Zinn

series ordinal

2

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23 April 2018

author name string

R L Prueitt

series ordinal

1

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23 April 2018

language of work or name

English

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publication date

1 February 2001

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23 April 2018

published in

Nature Genetics

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23 April 2018

volume

27

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23 April 2018

page(s)

132-134

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23 April 2018

issue

2

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23 April 2018

https://scigraph.springernature.com/pub.10.1038/84735

exact match

0 references

cites work

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

1 reference

7 January 2021

An association among blepharophimosis, resistant ovary syndrome, and true premature menopause

1 reference

7 January 2021

Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint

1 reference

7 January 2021

Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES.

1 reference

7 January 2021

Molecular Cytogenetic Evaluation in a Patient with a Translocation (3;21) Associated with Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome (BPES)

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Activin/inhibin beta B subunit gene disruption leads to defects in eyelid development and female reproduction.

1 reference

7 January 2021

Position effect in human genetic disease

1 reference

7 January 2021

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

1 reference

7 January 2021

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly

1 reference

7 January 2021

JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome

1 reference

7 January 2021

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

1 reference

7 January 2021

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

1 reference

7 January 2021

Identifiers

DOI

10.1038/84735

1 reference

23 April 2018

PubMed ID

11175772

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23 April 2018