(Q33596464)

28 July 2017

1 reference

title

Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'. (English)

1 reference

28 July 2017

4

Baraitser M

1 reference

28 July 2017

MacDermot KD

1

1 reference

28 July 2017

Winter RM

series ordinal

2

1 reference

28 July 2017

Taylor D

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 January 1991

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

28

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28 July 2017

issue

1

1 reference

28 July 2017

page(s)

18-26

1 reference

Facial paralysis in children: differential diagnosis.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016742

Hereditary congenital facial paralysis.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016742

Studies of malformation syndromes of man XXXXI B: Nosologic studies in the Hanhart and the Möbius syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016742

Three-generation pedigree of a Möbius syndrome variant with chromosome translocation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016742

Genetics of Mobius syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016742

CONGENITAL LARYNGEAL-ABDUCTOR PARALYSIS DUE TO NUCLEUS AMBIGUUS DYSGENESIS IN THREE BROTHERS.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016742

A family with Möbius syndrome

30 October 2018

1 reference

12 December 2020

Congenital Bilateral Facial Paralysis

1 reference

12 December 2020

Autosomal dominantly inherited cutis aplasia congenita, ear malformations, right-sided facial paresis, and dermal sinuses

1 reference

12 December 2020

Congenital facial diplegia

1 reference

12 December 2020

Heterogeneity and pleiotropism in the Moebius syndrome

1 reference

12 December 2020

Moebius syndrome in a child and extremity defect in her father

1 reference

12 December 2020

Facial weakness and oligosyndactyly: ? independent variable features of familial type of the Möbius syndrome

1 reference

12 December 2020

HEREDITARY PARALYSIS OF THE FACIAL NERVE

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.28.1.18

1 reference

28 July 2017

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28 July 2017

1 reference