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Literature DB >> 2995232

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

B Zoll, J Arnemann, M Krawczak, D N Cooper, G Pescia, W Wahli, P Steinbach, J Schmidtke.

Abstract

Linkage between the loci for fraXq of Martin-Bell syndrome and factor IX was studied in nine families exhibiting this syndrome by means of a restriction fragment length polymorphism at the factor IX locus. Computer analysis of the data indicates there to be no evidence for close linkage between the syndrome and the factor IX locus.

Entities: Disease

Mesh：

Substances：

Year: 1985 PMID： 2995232 DOI： 10.1007/bf00283366

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

33 in total

1. Transmission of fragile (X) (q27) site from a male.

Authors: G C Webb; J G Rogers; D B Pitt; J Halliday; T Theobald
Journal: Lancet Date: 1981-11-28 Impact factor: 79.321

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. Prenatal diagnosis of X-linked mental retardation with fragile (X) using fetoscopy and fetal blood sampling.

Authors: T Webb; C M Gosden; C H Rodeck; M A Hamill; P E Eason
Journal: Prenat Diagn Date: 1983 Apr-Jun Impact factor: 3.050

4. Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

Authors: G Camerino; K H Grzeschik; M Jaye; H De La Salle; P Tolstoshev; J P Lecocq; R Heilig; J L Mandel
Journal: Proc Natl Acad Sci U S A Date: 1984-01 Impact factor: 11.205

5. 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

6. 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

Review 7. The fragile X syndrome: the patients and their chromosomes.

Authors: M A De Arce; A Kearns
Journal: J Med Genet Date: 1984-04 Impact factor: 6.318

8. 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

9. Molecular cloning of the gene for human anti-haemophilic factor IX.

Authors: K H Choo; K G Gould; D J Rees; G G Brownlee
Journal: Nature Date: 1982-09-09 Impact factor: 49.962

10. Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

Authors: G Turner; R Brookwell; A Daniel; M Selikowitz; M Zilibowitz
Journal: N Engl J Med Date: 1980-09-18 Impact factor: 91.245

8 in total

1. Estimating the stability of the proposed imprinted state of the fragile-X mutation when transmitted by females.

Authors: P J Follette; C D Laird
Journal: Hum Genet Date: 1992-01 Impact factor: 4.132

2. Multilocus analysis of the fragile X syndrome.

Authors: W T Brown; A Gross; C Chan; E C Jenkins; J L Mandel; I Oberlé; B Arveiler; G Novelli; S Thibodeau; R Hagerman
Journal: Hum Genet Date: 1988-03 Impact factor: 4.132

3. 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