(Q48682109)

14 February 2018

title

Spectrum of the acrocallosal syndrome (English)

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14 February 2018

author name string

Rainer Koenig

1

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14 February 2018

Alexia Bach

2

1 reference

14 February 2018

Ulrike Woelki

3

1 reference

14 February 2018

Karl-Heinz Grzeschik

4

1 reference

14 February 2018

Sigrun Fuchs

5

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14 February 2018

publication date

1 February 2002

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14 February 2018

American Journal of Medical Genetics Part A

published in

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14 February 2018

volume

108

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14 February 2018

issue

1

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14 February 2018

page(s)

7-11

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14 February 2018

The acrocallosal syndrome and Greig syndrome are not allelic disorders

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Acrocallosal syndrome: additional manifestations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Acrocallosal syndrome in an Algerian boy born to consanguineous parents: review of the literature and further delineation of the syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

The variable clinical spectrum and mental prognosis of the acrocallosal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Further delineation of the acrocallosal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Acrocallosal syndrome: report of a Brazilian girl

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Fronto-nasal dysostosis, callosal agenesis, crossed-fused ectopia, tibial hemimelia, and preaxial polydactyly of feet: severe expression of the acrocallosal syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Acrocallosal syndrome: association with cystic malformation of the brain and neurodevelopmental aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum: an example of the variable clinical spectrum of the Acrocallosal syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

21 January 2018

Acrocallosal syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Recurrent anencephaly as a primary manifestation of the acrocallosal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Acrocallosal syndrome: new findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

Acrocallosal syndrome in a girl born to consanguineous parents

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10236

21 January 2018

Identifiers

DOI

10.1002/AJMG.10236

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14 February 2018

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14 February 2018