(Q35889343)

English

Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

scientific article published in May 1994

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scholarly article

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26 October 2019

Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8178816%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

author name string

Leana-Cox J

1

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26 October 2019

Jenkins L

2

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26 October 2019

Palmer CG

3

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26 October 2019

Plattner R

4

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26 October 2019

Sheppard L

5

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26 October 2019

Flejter WL

6

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26 October 2019

Zackowski J

7

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26 October 2019

Tsien F

8

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26 October 2019

Schwartz S

9

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26 October 2019

language of work or name

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publication date

1 May 1994

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26 October 2019

American Journal of Human Genetics

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26 October 2019

54

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26 October 2019

5

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26 October 2019

748-756

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26 October 2019

Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Clinical and molecular analysis of five inv dup(15) patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Preferential maternal derivation in inv dup(15): analysis of eight new cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Forty four probands with an additional "marker" chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Identification of two distinct subfamilies of alpha satellite DNA that are highly specific for human chromosome 15.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Identification of a marker chromosome as inv dup(15) by molecular analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Cytogenetic and clinical studies in five cases of inv dup(15)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918252

11 July 2018

The genetic significance of accessory bisatellited marker chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reflections on small supernumerary (marker) chromosomes: could imprinting and isodisomy play a role in the phenotypic expression of hyperdiploidy?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution banding in chromosomes of B lymphoblastoid cells and cultured skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A G-band study of chromosomes in liveborn infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome and a bisatellited derivative of chromosome 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An extra idic(15p)(q11) chromosome in Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal detection of an accessory chromosome identified as an inversion duplication (15)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8178816%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8178816%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

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