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Literature DB >> 1870092

X linked mental retardation.

I A Glass¹.

Abstract

Entities: Disease

Mesh：

Year: 1991 PMID： 1870092 PMCID： PMC1016899 DOI： 10.1136/jmg.28.6.361

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

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128 in total

1. Aarskog syndrome: full male and female expression associated with an X-autosome translocation.

Authors: E Bawle; M Tyrkus; S Lipman; D Bozimowski
Journal: Am J Med Genet Date: 1984-03

2. The marker (X) syndrome: a cytogenetic and genetic analysis.

Authors: S L Sherman; N E Morton; P A Jacobs; G Turner
Journal: Ann Hum Genet Date: 1984-01 Impact factor: 1.670

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

Authors: L B Holmes; D L Gang
Journal: Am J Med Genet Date: 1984-01

4. X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report.

Authors: J F Mattei; P Collignon; S Ayme; F Giraud
Journal: Clin Genet Date: 1983-01 Impact factor: 4.438

5. X linked recessive inheritance of agenesis of the corpus callosum.

Authors: P Kaplan
Journal: J Med Genet Date: 1983-04 Impact factor: 6.318

6. X-linked dominant inherited diseases with lethality in hemizygous males.

Authors: R Wettke-Schäfer; G Kantner
Journal: Hum Genet Date: 1983 Impact factor: 4.132

7. Mild mental retardation in children in a northern Swedish county.

Authors: H K Blomquist; K H Gustavson; G Holmgren
Journal: J Ment Defic Res Date: 1981-09

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

Authors: M Golabi; M Ito; B D Hall
Journal: Am J Med Genet Date: 1984-01

9. Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literature.

Authors: M Münke; K Kruse; M Goos; H H Ropers; M Tolksdorf
Journal: Eur J Pediatr Date: 1983-10 Impact factor: 3.183

10. Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation.

Authors: H H Ropers; O Zuffardi; E Bianchi; L Tiepolo
Journal: Hum Genet Date: 1982 Impact factor: 4.132

21 in total

1. X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.

Authors: A L Christianson; R E Stevenson; C H van der Meyden; J Pelser; F W Theron; P L van Rensburg; M Chandler; C E Schwartz
Journal: J Med Genet Date: 1999-10 Impact factor: 6.318

X linked mental retardation.

1. Aarskog syndrome: full male and female expression associated with an X-autosome translocation.

2. The marker (X) syndrome: a cytogenetic and genetic analysis.

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

4. X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report.

5. X linked recessive inheritance of agenesis of the corpus callosum.

6. X-linked dominant inherited diseases with lethality in hemizygous males.

7. Mild mental retardation in children in a northern Swedish county.

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

9. Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literature.

10. Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation.

1. X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.

2. Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11.

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

4. Another dystonia.

5. X-linked mental retardation: in pursuit of a gene map.

6. Linkage mapping of a severe X-linked mental retardation syndrome.

7. The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21).

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

9. Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosa.

Review 10. The FMR1 gene and fragile X-associated tremor/ataxia syndrome.