Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance (Q33680868)

28 July 2017

title

Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance (English)

1 reference

28 July 2017

Barber JC

1

1 reference

28 July 2017

Joyce CA

2

1 reference

28 July 2017

Collinson MN

3

1 reference

28 July 2017

Nicholson JC

4

1 reference

28 July 2017

Willatt LR

5

1 reference

28 July 2017

Dyson HM

6

1 reference

28 July 2017

Bateman MS

7

1 reference

28 July 2017

Green AJ

8

1 reference

28 July 2017

Yates JR

9

1 reference

28 July 2017

Dennis NR

10

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 June 1998

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

35

1 reference

28 July 2017

issue

6

1 reference

28 July 2017

page(s)

491-496

1 reference

A Correlation of Ring-Shaped Chromosomes with Variegation in Zea Mays

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Del(3) (p25.3) without phenotypic effect

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Identification of a C6-G21 translocation chromosome by the Q-M and Giemsa banding techniques in a patient with Down's syndrome, with possible assignment of Gm locus.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

A simple salting out procedure for extracting DNA from human nucleated cells

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

High-resolution R-banding at the 1250-band level. II. Schematic representation and nomenclature of human RBG-banded chromosomes.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Chromosome imbalance, normal phenotype, and imprinting

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Routine use of methods for improved G-band resolution in a population of patients with malformations and developmental delay

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Prenatal ascertainment of an inherited dup(18p) associated with an apparently normal phenotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Structural differences in reciprocal translocations. Potential for a model of risk in Rcp

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051344

Familial marker chromosome due to 3:1 disjunction of t(9;15) in a grandparent

30 October 2018

1 reference

12 December 2020

Deletion of band 13q21 is compatible with normal phenotype

1 reference

12 December 2020

Form of 15q proximal duplication appears to be a normal euchromatic variant

1 reference

12 December 2020

Fetal detection of dup 9p11-12

1 reference

12 December 2020

Euchromatic heteromorphism or duplication without phenotypic effect?

1 reference

12 December 2020

Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma

1 reference

12 December 2020

Fluorodeoxyuridine synchronization of bone marrow cultures

1 reference

12 December 2020

A rare inherited euchromatic heteromorphism on chromosome 1

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

Duplication of euchromatin without phenotypic effects: a variant of chromosome 16

1 reference

12 December 2020

Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.35.6.491

1 reference

28 July 2017

1 reference

28 July 2017

1 reference