(Q40269627)

19 September 2017

title

Miller-Dieker syndrome: lissencephaly and monosomy 17p. (English)

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Miller–Dieker lissencephaly syndrome

19 September 2017

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author

William B. Dobyns

1

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19 September 2017

Stratton RF

2

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19 September 2017

Parke JT

3

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19 September 2017

Greenberg F

4

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19 September 2017

Nussbaum RL

5

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19 September 2017

Ledbetter DH

6

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19 September 2017

language of work or name

English

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publication date

1 April 1983

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The Journal of Pediatrics

19 September 2017

published in

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19 September 2017

volume

102

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19 September 2017

issue

4

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19 September 2017

page(s)

552-558

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LISSENCEPHALY IN 2 SIBLINGS.

19 September 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

Agyria-pachygyria (lissencephaly syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

Lissencephaly (Agyria) on Computed Tomography

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

High Resolution of Human Chromosomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

A rapid banding technique for human chromosomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

Ring 17 chromosome detected by amniocentesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

Brief clinical report: ring chromosome 17 in a mentally retarded young man - clinical, cytogenetic, and biochemical investigations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

Langer-Giedion syndrome and deletion of the long arm of chromosome 8

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

Langer-Giedion syndrome with interstitial 8q-deletion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

A deletion in chromosome 22 can cause DiGeorge syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

inferred from DOI database lookup

7 January 2021

based on heuristic

An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980183-8

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(83)80183-8

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19 September 2017

1 reference