(Q53816487)

20 May 2018

title

New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13. (English)

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20 May 2018

Miller–Dieker lissencephaly syndrome

main subject

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author

William B. Dobyns

2

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20 May 2018

author name string

R F Stratton

1

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20 May 2018

S D Airhart

3

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20 May 2018

D H Ledbetter

4

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20 May 2018

publication date

1 January 1984

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20 May 2018

published in

Human Genetics

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20 May 2018

volume

67

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20 May 2018

page(s)

193-200

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20 May 2018

issue

2

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20 May 2018

https://scigraph.springernature.com/pub.10.1007/bf00273000

exact match

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cites work

The MIller-Dieker syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Langer-Giedion syndrome and additional congenital malformations with interstitial deletion of the long arm of chromosome 8 46, XY, del 8 (q 13-22)

1 reference

12 December 2020

A deletion in chromosome 22 can cause DiGeorge syndrome

1 reference

12 December 2020

An international system for human cytogenetic nomenclature--high-resolution banding (1981). ISCN (1981). Report of the Standing Committee on Human Cytogenetic Nomenclature

1 reference

12 December 2020

Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: localization on a single chromosome

1 reference

12 December 2020

A spectrum of gyral anomalies in Miller-Dieker (lissencephaly) syndrome

1 reference

12 December 2020

Ring chromosome 17 in a mentally retarded boy

1 reference

12 December 2020

LISSENCEPHALY IN 2 SIBLINGS.

1 reference

12 December 2020

Ring 17 chromosome detected by amniocentesis

1 reference

12 December 2020

Chromosome deletion and multiple cartilaginous exostoses

1 reference

12 December 2020

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

1 reference

12 December 2020

Agyria-pachygyria (lissencephaly syndrome)

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Miller-Dieker syndrome: lissencephaly and monosomy 17p.

1 reference

12 December 2020

1 reference

12 December 2020

Lissencephaly: two cases

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12 December 2020

Chromosome 17 has a real fragile site at p12

1 reference

12 December 2020

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

1 reference

12 December 2020

Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer Gene

1 reference

12 December 2020

A case of ring chromosome E 17: 46, XX, r(17) (p13 yields q25) (author's transl)

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00273000

1 reference

20 May 2018

PubMed ID

6745939

1 reference

20 May 2018