(Q36840945)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8986287%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

FISH characterization of small supernumerary marker chromosomes in two Prader-Willi patients (English)

1 reference

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22 October 2019

1

1 reference

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22 October 2019

author name string

N Rizzi

2

1 reference

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22 October 2019

D Giardino

3

1 reference

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22 October 2019

F Gurrieri

4

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22 October 2019

G Silvestri

5

1 reference

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22 October 2019

G Grugni

6

1 reference

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22 October 2019

L Larizza

7

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22 October 2019

publication date

1 January 1997

1 reference

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American Journal of Medical Genetics Part A

22 October 2019

published in

1 reference

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22 October 2019

volume

68

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22 October 2019

issue

1

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22 October 2019

page(s)

99-104

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Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization

22 October 2019

cites work

1 reference

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Identification of marker chromosomes in thirteen patients using FISH probing

21 January 2018

1 reference

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Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis

21 January 2018

1 reference

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Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

21 January 2018

1 reference

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Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescencein situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970110%2968%3A1%3C99%3A%3AAID-AJMG21%3E3.0.CO%3B2-I

A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12,699 prenatal samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970110%2968%3A1%3C99%3A%3AAID-AJMG21%3E3.0.CO%3B2-I

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970110%2968%3A1%3C99%3A%3AAID-AJMG21%3E3.0.CO%3B2-I

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970110%2968%3A1%3C99%3A%3AAID-AJMG21%3E3.0.CO%3B2-I

Marker chromosomes in a series of 10,000 prenatal diagnoses. Cytogenetic and follow-up studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970110%2968%3A1%3C99%3A%3AAID-AJMG21%3E3.0.CO%3B2-I

A small supernumerary marker chromosome X identified by in situ hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970110%2968%3A1%3C99%3A%3AAID-AJMG21%3E3.0.CO%3B2-I

Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11–q13

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970110%2968%3A1%3C99%3A%3AAID-AJMG21%3E3.0.CO%3B2-I

An imprinted gene(s) for diabetes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970110%2968%3A1%3C99%3A%3AAID-AJMG21%3E3.0.CO%3B2-I

Prader-Willi syndrome and a bisatellited derivative of chromosome 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970110%2968%3A1%3C99%3A%3AAID-AJMG21%3E3.0.CO%3B2-I

10.1002/(SICI)1096-8628(19970110)68:1<99::AID-AJMG21>3.0.CO;2-I

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8986287%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference