(Q36767578)

16 August 2017

Heteromorphic variants of chromosome 9 (English)

1 reference

16 August 2017

Nadezda Kosyakova

1

1 reference

16 August 2017

Ani Grigorian

2

1 reference

16 August 2017

Thomas Liehr

3

1 reference

16 August 2017

Marina Manvelyan

4

1 reference

16 August 2017

Isabella Simonyan

5

1 reference

16 August 2017

Hasmik Mkrtchyan

6

1 reference

16 August 2017

Rouben Aroutiounian

7

1 reference

16 August 2017

Anna D Polityko

8

1 reference

16 August 2017

Anna I Kulpanovich

9

1 reference

16 August 2017

Tatiana Egorova

10

1 reference

16 August 2017

Evgenia Jaroshevich

11

1 reference

16 August 2017

Alla Frolova

12

1 reference

16 August 2017

Natalia Shorokh

13

1 reference

16 August 2017

Irina V Naumchik

14

1 reference

16 August 2017

Marianne Volleth

15

1 reference

16 August 2017

Isolde Schreyer

16

1 reference

16 August 2017

Heike Nelle

17

1 reference

16 August 2017

Markus Stumm

18

1 reference

16 August 2017

Rolf-Dieter Wegner

19

1 reference

16 August 2017

Gisela Reising-Ackermann

20

1 reference

16 August 2017

Martina Merkas

21

1 reference

16 August 2017

Lukretija Brecevic

22

1 reference

16 August 2017

Thomas Martin

23

1 reference

16 August 2017

Laura Rodríguez

24

1 reference

16 August 2017

Samarth Bhatt

25

1 reference

16 August 2017

Monika Ziegler

26

1 reference

16 August 2017

Katharina Kreskowski

27

1 reference

16 August 2017

Anja Weise

28

1 reference

16 August 2017

Ali Sazci

29

1 reference

16 August 2017

Svetlana Vorsanova

30

1 reference

16 August 2017

Marcelo de Bello Cioffi

31

1 reference

16 August 2017

Emel Ergul

32

1 reference

16 August 2017

1 April 2013

1 reference

16 August 2017

Molecular Cytogenetics

1 reference

16 August 2017

6

1 reference

16 August 2017

1

1 reference

16 August 2017

14

1 reference

https://scigraph.springernature.com/pub.10.1186/1755-8166-6-14

16 August 2017

0 references

cites work

A new multicolor fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Sperm DNA integrity and meiotic behavior assessment in an infertile male carrier of a 9qh+++ polymorphism.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Novel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

The euchromatic 9p+ polymorphism is a locus-specific amplification caused by repeated copies of a small DNA segment mapping within 9p12.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Molecular topography of the secondary constriction region (qh) of human chromosome 9 with an unusual euchromatic band

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Complete deficiency of constitutive heterochromatin on a human chromosome 9

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Chromosome segregation in a man heterozygous for a pericentric inversion, inv(9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization on sperm nuclei.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Breakpoints in alpha, beta, and satellite III DNA sequences of chromosome 9 result in a variety of pericentric inversions

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Male infertility related to an aberrant karyotype, 46,XY,9ph,9qh+.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

A case-control study identifying chromosomal polymorphic variations as forms of epigenetic alterations associated with the infertility phenotype

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

TEM, FISH and molecular studies in infertile men with pericentric inversion of chromosome 9.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Acquired inv(9): what is its significance?

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

A total population study of diagnosed chromosome abnormalities in Queensland, Australia.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626942

Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation

5 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1755-8166-6-14

Extreme variant of enlarged heterochromatin region on chromosome 9Q in a normal child and multiple family members

21 January 2018

1 reference

12 December 2020

Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line

1 reference

12 December 2020

Extra G-positive band at chromosome 9q13 as a recurrent heteromorphism in a Korean population

1 reference

12 December 2020

Absence of pericentromeric heterochromatin (9qh-) in a patient with bilateral retinoblastoma

1 reference

12 December 2020

Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism

1 reference

12 December 2020

Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9

1 reference

12 December 2020

Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9

1 reference

12 December 2020

Euchromatic 9q13-q21 duplication variants are tandem segmental amplifications of sequence reciprocal to 9q13-q21 deletions

1 reference

12 December 2020

Identifiers

DOI

10.1186/1755-8166-6-14

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

23547710

1 reference