(Q36442424)

English

Further delineation of the acrocallosal syndrome

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Further delineation of the acrocallosal syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

author name string

Z Gelman-Kohan

1

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

J Antonelli

2

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

H Ankori-Cohen

3

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

H Adar

4

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

J Chemke

5

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

publication date

1 September 1991

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

150

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

797-799

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

The acrocallosal syndrome in first cousins: widening of the spectrum of clinical features and further support for autosomal recessive inheritance

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The acrocallosal syndrome in sisters.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The acrocallosal syndrome in a Turkish boy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication of hands and feet, multiple joint dislocations, absence of corpus callosum and hypsarrhythmia: acrocallosal syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The acrocallosal syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Could acrocallosal syndrome and Greig syndrome affect the same developmental gene?

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The acrocallosal syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acrocallosal syndrome: new findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acrocallosal syndrome: additional manifestations

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New and old syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acrocallosal syndrome in a girl born to consanguineous parents

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypogenitalism in the acrocallosal syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1659985

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02026715

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

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