(Q41127106)

27 September 2017

1 reference

title

XLMR genes: update 1996. (English)

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27 September 2017

Lubs HA

1

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27 September 2017

Chiurazzi P

2

1 reference

27 September 2017

Arena JF

3

1 reference

27 September 2017

Schwartz C

4

1 reference

27 September 2017

Tranebjaerg L

5

1 reference

27 September 2017

Neri G

6

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27 September 2017

publication date

1 July 1996

1 reference

American Journal of Medical Genetics Part A

27 September 2017

published in

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27 September 2017

volume

64

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27 September 2017

issue

1

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27 September 2017

page(s)

147-157

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

27 September 2017

cites work

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Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome

21 January 2018

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A new X-linked mental retardation syndrome

21 January 2018

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Congenital X-linked ataxia, progressive myoclonic encephalopathy, macular degeneration and recurrent infections

21 January 2018

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New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation

21 January 2018

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A candidate gene for mild mental handicap at the FRAXE fragile site

21 January 2018

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Prenatal diagnosis of Dandy-Walker malformation in a family displaying X-linked inheritance

21 January 2018

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Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22

21 January 2018

1 reference

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The clinical spectrum of mutations in L1, a neuronal cell adhesion molecule

21 January 2018

1 reference

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Mental retardation locus in Xp21 chromosome microdeletion

21 January 2018

1 reference

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Identification of the gene FMR2, associated with FRAXE mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Localisation of the MRX3 gene for non-specific X linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

21 January 2018

1 reference

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Linkage analysis in a large family with nonspecific X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

A new X-linked multiple congenital anomalies/mental retardation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Localization of a non-specific X-linked mental retardation gene, MRX23, to Xq23-q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Nonspecific X-linked mental retardation II: the frequency in British Columbia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Brief clinical report: an X-linked mental retardation syndrome with craniofacial abnormalities, microcephaly and club foot

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

A new X linked syndrome with mental retardation and craniofacial dysmorphism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Linkage of nonspecific X-linked mental retardation to Xq21.31.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

X-linked recessive inheritance of dysgenesis of corpus callosum in a Chinese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Localization of non-specific X-linked mental retardation genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Localization of a gene for X-linked nonspecific mental retardation (MRX24) in Xp22.2-p22.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

X-linked mental retardation syndrome: three brothers with the Brooks-Wisniewski-Brown syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

21 January 2018

XLMR genes: update 1992.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

21 January 2018

XLMR genes: update 1990.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Linkage to Xq28 in a family with nonspecific X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Physical mapping of DNA markers in the q13-q22 region of the human X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Gene for non-specific X-linked mental retardation maps in the pericentromeric region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

A high resolution deletion map of human chromosome Xp22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

MRX8: an X-linked mental retardation condition with linkage to Xq21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

X-linked syndrome: mental retardation, hip luxation, and G6PD variant [Gd(+) Butantan].

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

New X-linked syndrome of mental retardation, short stature, and hypertelorism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Recurrent myoglobinuria in a child with mental retardation: phosphoglycerate kinase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Mental retardation, acromegalic face, and megalotestes in two half-brothers: a specific form of X-linked mental retardation without fra(X) (q)?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

New X-linked syndrome with apraxia, ataxia, and mental deficiency: Clinical, cytogenetic and neuropsychological studies in two Danish families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

X-linked hypogonadism, gynecomastia, mental retardation, short stature, and obesity--a new syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

XNP mutation in a large family with Juberg-Marsidi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

X-linked myotubular myopathy: clinical observations in ten additional cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Craniofrontonasal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Refined localization of the Prieto-syndrome locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

21 January 2018

XLMR genes: update 1994

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

Further linkage evidence for localization of mutational sites for nonsyndromic types of X-linked mental retardation at the pericentromeric region

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960712%2964%3A1%3C147%3A%3AAID-AJMG25%3E3.0.CO%3B2-M

10.1002/(SICI)1096-8628(19960712)64:1<147::AID-AJMG25>3.0.CO;2-M

21 January 2018

Identifiers

DOI

1 reference

27 September 2017

1 reference