(Q41134121)

27 September 2017

title

Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations (English)

1 reference

26 October 2022

1 reference

1 reference

26 October 2022

author name string

N. Archidiacono

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673961

26 October 2022

M. Lerone

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673961

26 October 2022

M. Rocchi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673961

26 October 2022

M. Anvret

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673961

26 October 2022

T. Ozcelik

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673961

26 October 2022

U. Francke

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673961

26 October 2022

G. Romeo

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673961

26 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1673961

26 October 2022

publication date

1 April 1991

1 reference

full work available at URL

27 September 2017

http://link.springer.com/content/pdf/10.1007/BF00201549.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00201549/fulltext.html

26 October 2022

1 reference

http://link.springer.com/content/pdf/10.1007/BF00201549

26 October 2022

1 reference

26 October 2022

1 reference

27 September 2017

volume

86

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27 September 2017

issue

6

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27 September 2017

page(s)

604-606

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Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids

27 September 2017

cites work

1 reference

12 December 2020

Report of the committee on the genetic constitution of the X and Y chromosomes

1 reference

12 December 2020

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

1 reference

12 December 2020

The clinical pattern of the Rett syndrome

1 reference

12 December 2020

A de novo X;3 translocation in Rett syndrome

1 reference

12 December 2020

Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations

1 reference

12 December 2020

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

12 December 2020

[On the genetics of incontinentia pigmenti.]

1 reference

12 December 2020

The genetics of Rett syndrome: the consequences of a disorder where every case is a new mutation

1 reference

12 December 2020

Report of the committee on the genetic constitution of the X chromosome

1 reference

12 December 2020

A simple method for fusing human lymphocytes with rodent cells in monolayer by polyethylene glycol

1 reference

12 December 2020

Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X.

1 reference

12 December 2020

Rett syndrome--search for genetic markers.

1 reference

12 December 2020

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

1 reference

12 December 2020

A monozygotic twin pair with Rett syndrome

1 reference

12 December 2020

Chromosome findings in the Rett syndrome and a test of a two-step mutation theory

1 reference

12 December 2020

On the genetics of Rett syndrome: analysis of family and pedigree data.

1 reference

12 December 2020

Easy calculations of lod scores and genetic risks on small computers

1 reference

12 December 2020

Report of the committee on the genetic constitution of the X chromosome

1 reference

12 December 2020

Selection against lethal alleles in females heterozygous for incontinentia pigmenti

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00201549

1 reference

Dimensions Publication ID

27 September 2017

1030781338

0 references

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