Literature DB >> 2411652

A new MspI restriction fragment length polymorphism in the hemophilia B locus.

G Camerino, I Oberlé, D Drayna, J L Mandel.   

Abstract

Using a partial cDNA probe for human coagulation factor IX, we have detected a new restriction fragment length polymorphism in human DNA digested with MspI. The frequency of the minor allele is 0.20 +/- 0.05 and average heterozygosity is about 0.32. The MspI RFLP is in strong linkage disequilibrium with the TaqI RFLP previously described, but should nevertheless be useful in segregation analysis in case of homozygosity for the TaqI minor allele.

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Year:  1985        PMID： 2411652     DOI： 10.1007/bf00295673

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


  11 in total

1.  Exclusion of haemophilia B in male fetus by chorionic villus biopsy.

Authors:  T Tønnesen; F Søndergaard; F Güttler; I Oberlé; J P Moisan; J L Mandel; M Hauge; E M Damsgård
Journal:  Lancet       Date:  1984-10-20       Impact factor: 79.321

2.  Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome.

Authors:  I Oberlé; J L Mandel; J Boué; M G Mattei; J F Mattei
Journal:  Lancet       Date:  1985-04-13       Impact factor: 79.321

3.  Nonrandom association of polymorphic restriction sites in the beta-globin gene cluster.

Authors:  S E Antonarakis; C D Boehm; P J Giardina; H H Kazazian
Journal:  Proc Natl Acad Sci U S A       Date:  1982-01       Impact factor: 11.205

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.  Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Authors:  D Drayna; K Davies; D Hartley; J L Mandel; G Camerino; R Williamson; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

6.  Regional localization of the human factor IX gene by molecular hybridization.

Authors:  P F Chance; K A Dyer; K Kurachi; S Yoshitake; H H Ropers; P Wieacker; S M Gartler
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

Authors:  F Giannelli; D S Anson; K H Choo; D J Rees; P R Winship; N Ferrari; C R Rizza; G G Brownlee
Journal:  Lancet       Date:  1984-02-04       Impact factor: 79.321

8.  Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.

Authors:  G Camerino; M G Mattei; J F Mattei; M Jaye; J L Mandel
Journal:  Nature       Date:  1983 Dec 15-21       Impact factor: 49.962

9.  Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome.

Authors:  Y Boyd; V J Buckle; E A Munro; K H Choo; B R Migeon; I W Craig
Journal:  Ann Hum Genet       Date:  1984-05       Impact factor: 1.670

10.  The gene structure of human anti-haemophilic factor IX.

Authors:  D S Anson; K H Choo; D J Rees; F Giannelli; K Gould; J A Huddleston; G G Brownlee
Journal:  EMBO J       Date:  1984-05       Impact factor: 11.598
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  16 in total

1.  Defining DNA diagnostic tests appropriate or standard clinical care.

Authors:  R V Lebo; G Cunningham; M J Simons; L J Shapiro
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

2.  MspI polymorphic site within the factor IX gene. Localization of the site and an improved method for detection.

Authors:  D L Freedenberg; S H Chen; K Kurachi; C R Scott
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

3.  An HhaI polymorphism is present in factor IX genes of Asian subjects.

Authors:  A P Reiner; A R Thompson
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

4.  Diagnosis of haemophilia B using the polymerase chain reaction.

Authors:  J Reiss; U Neufeldt; K Wieland; B Zoll
Journal:  Blut       Date:  1990-01

5.  Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome.

Authors:  I Oberlé; G Camerino; C Kloepfer; J P Moisan; K H Grzeschik; B Hellkuhl; M C Hors-Cayla; N Van Cong; D Weil; J L Mandel
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

6.  A DNA marker closely linked to the factor IX (haemophilia B) gene.

Authors:  L Mulligan; J J Holden; B N White
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

7.  Population genetics of coagulant factor IX: frequencies of two DNA polymorphisms in five ethnic groups.

Authors:  D B Lubahn; S T Lord; J Bosco; J Kirshtein; O J Jeffries; N Parker; C Levtzow; L M Silverman; J B Graham
Journal:  Am J Hum Genet       Date:  1987-06       Impact factor: 11.025

8.  Human Xq24-Xq28: approaches to mapping with yeast artificial chromosomes.

Authors:  M Wada; R D Little; F Abidi; G Porta; T Labella; T Cooper; G Della Valle; M D'Urso; D Schlessinger
Journal:  Am J Hum Genet       Date:  1990-01       Impact factor: 11.025

9.  Hemophilia B (Christmas disease) variants and carrier detection analyzed by DNA probes.

Authors:  M C Poon; D H Chui; M Patterson; D M Starozik; L S Dimnik; D I Hoar
Journal:  J Clin Invest       Date:  1987-04       Impact factor: 14.808

10.  Variations among Japanese of the factor IX gene (F9) detected by PCR-denaturing gradient gel electrophoresis.

Authors:  C Satoh; N Takahashi; J Asakawa; K Hiyama; M Kodaira
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025
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