(Q33677795)

28 July 2017

Rett syndrome, classical and atypical: genealogical support for common origin (English)

1 reference

28 July 2017

0 references

2

B Hagberg

0 references

author name string

H O Akesson

series ordinal

1

1 reference

PubMed ID

8880578

28 July 2017

J Wahlström

series ordinal

3

1 reference

PubMed ID

8880578

28 July 2017

language of work or name

English

0 references

publication date

1 September 1996

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

33

1 reference

28 July 2017

9

1 reference

28 July 2017

764-766

1 reference

Rett syndrome: clinical peculiarities and biological mysteries

28 July 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050732

Rett syndrome: A search for gene sources

14 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050732

Rett variants: a suggested model for inclusion criteria.

14 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050732

Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescence

30 October 2018

1 reference

12 December 2020

Neurofibromatosis in Gothenburg, Sweden. IV. Genetic analyses

1 reference

12 December 2020

Another model for the inheritance of Rett syndrome

1 reference

12 December 2020

Rett syndrome: potential gene sources--phenotypical variability

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.33.9.764

1 reference

28 July 2017

1 reference

28 July 2017

1 reference

PubMed ID

8880578