(Q34263804)

1 August 2017

title

Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men (English)

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1 August 2017

5

Ankita Patel

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1 August 2017

Alexander N Yatsenko

1

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1 August 2017

Svetlana A Yatsenko

2

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1 August 2017

John W Weedin

3

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1 August 2017

Amy E Lawrence

4

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1 August 2017

Sandra Peacock

6

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1 August 2017

Martin M Matzuk

7

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1 August 2017

Dolores J Lamb

8

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1 August 2017

Sau Wai Cheung

9

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1 August 2017

Larry I Lipshultz

10

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1 August 2017

language of work or name

English

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publication date

20 February 2010

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1 August 2017

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1 August 2017

volume

183

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1 August 2017

issue

4

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1 August 2017

page(s)

1636-1642

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The biology of infertility: research advances and clinical challenges

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Underlying karyotype abnormalities in IVF/ICSI patients

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Risk of transmission of genetic diseases by assisted reproduction

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Klinefelter syndrome in clinical practice

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Chromosome abnormalities in one thousand infertile males with nonobstructive sperm disorders.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10 mutations in oligozoospermic patients impair homodimerization

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Male factor infertility: evaluation and management

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Azoospermia in patients heterozygous for a mutation in SYCP3

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

A multitude of genes expressed solely in meiotic or postmeiotic spermatogenic cells offers a myriad of contraceptive targets

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Fertility, family planning, and women's health: new data from the 1995 National Survey of Family Growth

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Robertsonian translocation and their role in pathogenesis of recurrent in vitro fertilization failure

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Sperm ultrastructure and meiotic segregation in an infertile 47, XYY man.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Sperm aneuploidy and meiotic sex chromosome configurations in an infertile XYY male.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Prevalence of chromosomal abnormalities in phenotypically normal and fertile adult males: large-scale survey of over 10,000 sperm donor karyotypes.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

An SNP in protamine 1: a possible genetic cause of male infertility?

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Guidelines for the appropriate use of genetic tests in infertile couples.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

An excess of chromosome 1 breakpoints in male infertility

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2969182

Assessment of sex chromosome aneuploidy in sperm nuclei from 47,XXY and 46,XY/47,XXY males: comparison with fertile and infertile males with normal karyotype

28 October 2018

1 reference

12 December 2020

Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome

1 reference

12 December 2020

Cytogenetic analysis of azoospermic patients: karyotype comparison of peripheral blood lymphocytes and testicular tissue

1 reference

12 December 2020

Evaluation of the azoospermic male

1 reference

12 December 2020

Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men

1 reference

12 December 2020

10.1016/J.JURO.2009.12.004

Identifiers

DOI

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1 August 2017

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1 August 2017

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