(Q57398176)

20

object named as

Doron Lancet

0 references

author name string

Nili Avidan

1

0 references

Hannah Tamary

2

0 references

Orly Dgany

3

0 references

Daniel Cattan

4

0 references

Alexandre Pariente

5

0 references

Michel Thulliez

6

0 references

Nicolas Borot

7

0 references

Lucien Moati

8

0 references

Alain Barthelme

9

0 references

Lea Shalmon

10

0 references

Tatyana Krasnov

11

0 references

Edna Ben-Asher

12

0 references

Tsvyia Olender

13

0 references

Miriam Khen

14

0 references

Issac Yaniv

15

0 references

Rina Zaizov

16

0 references

Hanna Shalev

17

0 references

Jean Delaunay

18

0 references

Marc Fellous

European Journal of Human Genetics

19

0 references

publication date

27 June 2003

0 references

published in

0 references

volume

11

0 references

issue

7

0 references

page(s)

497-502

0 references

cites work

Cloning and sequencing of human FSH receptor cDNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

The frequency of androgen receptor deficiency in infertile men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

The immotile-cilia syndrome. A congenital ciliary abnormality as an etiologic factor in chronic airway infections and male sterility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

A sperm ion channel required for sperm motility and male fertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

A voltage-gated ion channel expressed specifically in spermatozoa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

A new DNA sequence assembly program

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Basic local alignment search tool

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

The PROSITE database, its status in 2002

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Increased coverage of protein families with the blocks database servers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Recent segmental duplications in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

Genome architecture, rearrangements and genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

The androgen receptor gene mutations database

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

7 January 2021

Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

7 January 2021

'9 + 0' axoneme in spermatozoa and some nasal cilia of a patient with totally immotile spermatozoa associated with thickened sheath and short midpiece

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

7 January 2021

Familial oligoasthenoteratozoospermia: evidence of autosomal dominant inheritance with sex-limited expression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

7 January 2021

Two-phase liquid culture system models normal human adult erythropoiesis at the molecular level

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

7 January 2021

Long RT-PCR Amplification of the entire coding sequence of the polycystic kidney disease 1 (PKD1) gene.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200991

7 January 2021