(Q24538917)

6 July 2017

title

Renpenning syndrome maps to Xp11. (English)

1 reference

6 July 2017

1 reference

R E Stevenson

1

1 reference

6 July 2017

J F Arena

2

1 reference

6 July 2017

E Ouzts

3

1 reference

6 July 2017

A Gibson

4

1 reference

6 July 2017

M H Shokeir

5

1 reference

6 July 2017

C Vnencak-Jones

6

1 reference

6 July 2017

H A Lubs

7

1 reference

6 July 2017

M May

8

1 reference

6 July 2017

C E Schwartz

9

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6 July 2017

language of work or name

English

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publication date

1 May 1998

1 reference

6 July 2017

number of pages

10

1 reference

American Journal of Human Genetics

inferred from page(s)

published in

1 reference

6 July 2017

volume

62

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6 July 2017

issue

5

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6 July 2017

page(s)

1092-1101

1 reference

Familial sex-linked mental retardation

6 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=1377092

A gene for dominant nonspecific X-linked mental retardation is located in Xq28

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

24 March 2017

A marker X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

A comprehensive genetic map of the human genome based on 5,264 microsatellites

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

X-linked mental retardation: Renpenning revisited

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Easy calculations of lod scores and genetic risks on small computers

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

7 April 2017

XLMR genes: update 1996.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Identification of the gene FMR2, associated with FRAXE mental retardation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Detection of clonal immunoglobulin heavy chain gene rearrangements by polymerase chain reaction in scrapings from archival hematoxylin and eosin-stained histologic sections: implications for molecular genetic studies of focal pathologic lesions

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Recessive sex-linked mental retardation in the absence of other recognizable abnormalities. Report of a family

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

X-linked mental retardation without physical abnormality (Renpenning's syndrome) in sibs in an institution.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Allan-Herndon syndrome. I. Clinical studies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Unique X-linked mental retardation syndrome with fingertip arches and contractures linked to Xq21.31.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Familial X-linked mental retardation, verbal disability, and marker X chromosomes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Renpenning's syndrome--X-linked mental retardation.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Letter: Sex-linked mental retardation.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Letter: Renpenning's syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families).

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

X-linked dysmorphic syndrome with mental retardation.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Hereditary mental defect showing the pattern of sex influence.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Fragile X-linked mental retardation: the Martin-Bell syndrome

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Developmental dyspraxia in a family with X-linked mental retardation (Renpenning syndrome).

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377092

Automation of genetic linkage analysis using fluorescent microsatellite markers

29 November 2018

1 reference

12 December 2020

Sixth International Workshop on Human X Chromosome Mapping 1995. Banff, Alberta, Canada, June 16-18, 1995. Report and abstracts

1 reference

12 December 2020

Identification by STS PCR screening of a microdeletion in Xp21.3-22.1 associated with non-specific mental retardation

1 reference

12 December 2020

+2.71 LOD score at zero recombination is not sufficient for establishing linkage between X-linked mental retardation and X-chromosome markers

1 reference

12 December 2020

How many X-linked genes for non-specific mental retardation (MRX) are there?

1 reference

12 December 2020

"Renpenning" syndrome

1 reference

12 December 2020

XLMR genes: Update 1998

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F301835

7 January 2021

inferred from DOI database lookup

X-linked Mental Retardation Without Physical Abnormality: Renpenning's Syndrome

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F301835

7 January 2021

inferred from DOI database lookup

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F301835

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/301835

1 reference

6 July 2017

1 reference

6 July 2017

1 reference