(Q34206620)

31 July 2017

title

Mutational analysis of the human FATE gene in 144 infertile men. (English)

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31 July 2017

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7

Niels Tommerup

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author name string

Christian Olesen

1

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31 July 2017

Joachim Silber

2

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31 July 2017

Hans Eiberg

3

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31 July 2017

Erik Ernst

4

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31 July 2017

Karsten Petersen

5

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31 July 2017

Svend Lindenberg

6

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31 July 2017

language of work or name

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14 June 2003

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31 July 2017

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31 July 2017

volume

113

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31 July 2017

issue

3

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31 July 2017

page(s)

195-201

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Every sperm is sacred: fertilization in Caenorhabditis elegans

31 July 2017

cites work

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12 December 2020

The human Y chromosome: a 43-interval map based on naturally occurring deletions

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12 December 2020

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene

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12 December 2020

Eighth International Workshop on Ataxia-Telangiectasia (ATW8)

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12 December 2020

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

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12 December 2020

Y chromosome microdeletions and alterations of spermatogenesis

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12 December 2020

Update of the androgen receptor gene mutations database

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12 December 2020

Mutations and polymorphisms in gonadotropin genes

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12 December 2020

Nomenclature for the description of human sequence variations

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12 December 2020

High incidence of single nucleotide substitutions in the mitochondrial genome is associated with poor semen parameters in men

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12 December 2020

Genetic risks of intracytoplasmic sperm injection in the treatment of male infertility: recommendations for genetic counseling and screening

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12 December 2020

Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility

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12 December 2020

Impact of genetic engineering on the understanding of spermatogenesis

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12 December 2020

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

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12 December 2020

Mutations of LH and FSH receptors.

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12 December 2020

The HUGO Gene Nomenclature Committee (HGNC).

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12 December 2020

Identification of human candidate genes for male infertility by digital differential display

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12 December 2020

Human FATE is a novel X-linked gene expressed in fetal and adult testis

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12 December 2020

Linkage between serum cholinesterase 2 (CHE2) and gamma-crystallin gene cluster (CRYG): assignment to chromosome 2.

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12 December 2020

Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome

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12 December 2020

Understanding the genes involved in spermatogenesis: a progress report

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12 December 2020

A new probably X-linked inherited syndrome: congenital muscular torticollis, multiple keloids cryptorchidism and renal dysplasia

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12 December 2020

Meiotic analysis of two human reciprocal X-autosome translocations

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12 December 2020

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

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12 December 2020

Defining regions of the Y-chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection

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12 December 2020

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y

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12 December 2020

Identification of a Y chromosome haplogroup associated with reduced sperm counts

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12 December 2020

Towards an understanding of the genetics of human male infertility: lessons from flies

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12 December 2020

Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, Mckusick) is at Xq28, distal to the G6PD locus

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12 December 2020

Deletion and expression analysis of AZFa genes on the human Y chromosome revealed a major role for DBY in male infertility

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12 December 2020

CFTR gene mutations and male infertility.

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12 December 2020

10.1007/S00439-003-0974-9

Identifiers

DOI

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Dimensions Publication ID

31 July 2017

1020507065

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