(Q33674701)

28 July 2017

1 reference

title

Inv dup(15) supernumerary marker chromosomes (English)

1 reference

28 July 2017

Webb T

1

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 August 1994

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

31

1 reference

28 July 2017

issue

8

1 reference

28 July 2017

page(s)

585-594

1 reference

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome

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=1050018

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Extra dicentric 15 pter leads to q21/22 chromosomes in five unrelated patients with a distinct syndrome of progressive psychomotor retardation, seizures, hyper-reactivity and dermatoglyphic abnormalities.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

The cytogenetic controversy in the Prader-Labhart-Willi syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

A 15 leads to 1 translocation in a patient mosaic for presence or absence of an isodic(15p)(q11).

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Inv dup (15) with mental retardation but few dysmorphic features

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Forty four probands with an additional "marker" chromosome.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Inv dup (15): prenatal diagnosis and postnatal follow-up.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Supernumary marker chromosomes in a mentally retarded population identified as inv dup(15).

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Structure, origin and effects of a supernumerary marker chromosome 15.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Chromosome findings in twins with early-onset autistic disorder.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Marker chromosomes: cytogenetic characterization and implications for prenatal diagnosis.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Uniparental paternal disomy in Angelman's syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Two extra inv dup(15) chromosomes and male infertility: second case

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

The origin and behavior of two isodicentric bisatellited chromosomes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050018

A case of Prader-Willi syndrome in a girl with a small extra chromosome

30 October 2018

1 reference

12 December 2020

Bisatellited extra small metacentric chromosome in newborns

1 reference

12 December 2020

Prader-Willi syndrome and chromosomal mosaicism 46,XY/47,XY,+mar in two cases

1 reference

12 December 2020

Parental origin of de novo chromosome rearrangements

1 reference

12 December 2020

Prader-Willi syndrome and a bisatellited derivative of chromosome 15

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Supernumerary chromosomes in six patients

1 reference

12 December 2020

The genetic significance of accessory bisatellited marker chromosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

Abnormal chromosome in Prader-Willi syndrome

1 reference

12 December 2020

High resolution pattern of an inverted duplication (15)

1 reference

12 December 2020

Infertility associated with two accessory bisatellited chromosomes

1 reference

12 December 2020

Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?

1 reference

12 December 2020

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

1 reference

12 December 2020

Recurrent neuroleptic malignant syndrome associated with inv dup(15) and mental retardation

1 reference

12 December 2020

Unique karyotypes in two patients with Prader-Willi syndrome

1 reference

12 December 2020

A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)

1 reference

12 December 2020

Initial experience with use of fibrin glue in the treatment of acute gastroduodenal hemorrhage

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.31.8.585

1 reference

28 July 2017

1 reference

28 July 2017

1 reference