(Q38497667)

3 September 2017

title

Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation (English)

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3 September 2017

Hand JL

1

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3 September 2017

Michels VV

2

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3 September 2017

Marinello MJ

3

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3 September 2017

Ketterling RP

4

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3 September 2017

Jalal SM

5

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3 September 2017

publication date

1 February 2000

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3 September 2017

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3 September 2017

volume

20

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3 September 2017

issue

2

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3 September 2017

page(s)

144-8; discussion 149-51

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Interstitial deletions without phenotypic effect: prenatal diagnosis of a new family and brief review

3 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

A chromosomal deletion map of human malformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

Mechanisms of chromosome banding and implications for chromosome structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

Molecular defects in genetic diseases of peroxisomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

Brief clinical report: del(X) (q26) in a phenotypically normal woman and her daughter who also has trisomy 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9

21 January 2018

Identifiers

DOI

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3 September 2017

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