(Q56231061)

English

Prenatal and postnatal investigation of a case with Miller-Dieker syndrome due to a familial cryptic translocation t(17;20) (p13.3;q13.3) detected by fluorescence in situ hybridization

scientific article published on 01 February 1997

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9061768%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Prenatal and postnatal investigation of a case with Miller-Dieker syndrome due to a familial cryptic translocation t(17;20) (p13.3;q13.3) detected by fluorescence in situ hybridization (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9061768%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Miller–Dieker lissencephaly syndrome

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author name string

S L van Zelderen-Bhola

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9061768%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

E J Breslau-Siderius

2

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1 November 2019

G C Beverstock

3

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1 November 2019

I Stolte-Dijkstra

4

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1 November 2019

L S de Vries

5

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1 November 2019

P Stoutenbeek

6

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1 November 2019

J M de Pater

7

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1 November 2019

publication date

1 February 1997

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1 November 2019

Prenatal Diagnosis

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1 November 2019

17

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1 November 2019

2

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1 November 2019

173-179

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1 November 2019

describes a project that uses

fluorescence in situ hybridization

1 reference

based on heuristic

inferred from title

Miller-Dieker syndrome: lissencephaly and monosomy 17p.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

The lissencephaly (agyria) syndrome in siblings. Computerized tomographic and neuropathologic findings

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

Familial half cryptic translocation t(9;17).

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridization

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

Miller-Dieker syndrome due to maternal cryptic translocation t(10;17) (q26.3;p13.3)

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

LISSENCEPHALY IN 2 SIBLINGS.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199702%2917%3A2%3C173%3A%3AAID-PD30%3E3.0.CO%3B2-V

21 January 2018

Identifiers

10.1002/(SICI)1097-0223(199702)17:2<173::AID-PD30>3.0.CO;2-V

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9061768%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9061768%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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