Literature DB >> 6371234

The fragile X syndrome: the patients and their chromosomes.

M A De Arce, A Kearns.   

Abstract

We have reviewed recent publications, mostly from 1980 onwards, concerned with the problem of identifying patients with the fragile X chromosome and mental retardation, considering the two practical sides of the problem, that is, identification by their external appearance and by chromosomal studies. We conclude that this condition covers a large range of physical findings which occur in varying degrees in people with the chromosome marker. We have tried to clarify the existent criteria that have to be considered for an accurate cytogenetic diagnosis.

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Year:  1984        PMID: 6371234      PMCID: PMC1049231          DOI: 10.1136/jmg.21.2.84

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


  69 in total

1.  Inherited congenital normofunctional testicular hyperplasia and mental deficiency.

Authors:  J M Cantú; H E Scaglia; M Medina; M González-Diddi; T Morato; M E Moreno; G Pérez-Palacios
Journal:  Hum Genet       Date:  1976-07-07       Impact factor: 4.132

2.  Marker X chromosomes and mental retardation.

Authors:  G R Sutherland
Journal:  N Engl J Med       Date:  1977-06-16       Impact factor: 91.245

3.  The fragile X: a scanning electron microscope study.

Authors:  C J Harrison; E M Jack; T D Allen; R Harris
Journal:  J Med Genet       Date:  1983-08       Impact factor: 6.318

4.  Screening for fra(X)(q) in a population of mentally retarded males.

Authors:  U Froster-Iskenius; G Felsch; C Schirren; E Schwinger
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  X-linked mental retardation and fragile-X or marker-X syndrome.

Authors:  F A Rhoads
Journal:  Pediatrics       Date:  1982-05       Impact factor: 7.124

6.  On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression.

Authors:  P Steinbach; G Barbi; T Böller
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

7.  X-linked mental retardation, macro-orchidism, and the Xq27 fragile site.

Authors:  G Turner; A Daniel; M Frost
Journal:  J Pediatr       Date:  1980-05       Impact factor: 4.406

8.  X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.

Authors:  K B Nielsen; N Tommerup; H Poulsen; M Mikkelsen
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Familial X-linked mental retardation with an X chromosome abnormality.

Authors:  J Harvey; C Judge; S Wiener
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

10.  Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1982-05       Impact factor: 11.025

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  6 in total

1.  Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX.

Authors:  B Zoll; J Arnemann; M Krawczak; D N Cooper; G Pescia; W Wahli; P Steinbach; J Schmidtke
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 2.  Molecular genetics of the human X chromosome.

Authors:  K E Davies
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

3.  Fragile X syndrome: clinical, cytogenetic, biochemical and molecular features.

Authors:  J C Mixon; V G Dev
Journal:  Indian J Pediatr       Date:  1986 Jul-Aug       Impact factor: 1.967

4.  Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome.

Authors:  G Barbi; P Steinbach; S Baur; W Vogel
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

5.  Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.

Authors:  J M Connor; L A Pirrit; J R Yates; J A Crossley; S J Imrie; J M Colgan
Journal:  J Med Genet       Date:  1987-01       Impact factor: 6.318

6.  Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

Authors:  L M Mulligan; M A Phillips; C J Forster-Gibson; J Beckett; M W Partington; N E Simpson; J J Holden; B N White
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

  6 in total

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