Literature DB >> 2985491

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.

M G Mattei, M A Baeteman, R Heilig, I Oberlé, K Davies, J L Mandel, J F Mattei.   

Abstract

The coagulation factor IX gene and two other polymorphic loci corresponding to DNA probes 52 A and St 14 have been previously localized in the q27 to qter region of the human X chromosome. In order to study their localization with respect to the fragile site at Xq27-28, we have hybridized the three DNA probes to metaphase chromosomes of a boy with fragile X mental retardation. We show that probe 52 A is located in the proximal part of the Xq27 band, while the coagulation factor IX gene is on the distal part of this band, but proximal to the fragile site. The very polymorphic St 14 probe is located in the distal part of the Xq28 band, on the other side of the fragile site.

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Year:  1985        PMID： 2985491     DOI： 10.1007/bf00291650

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


  17 in total

1.  The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.

Authors:  I Oberlé; D Drayna; G Camerino; R White; J L Mandel
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

2.  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

3.  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

4.  A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome.

Authors:  P A Jacobs; M Mayer; J Matsuura; F Rhoads; S C Yee
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  Chromosomal localization of the human placental lactogen-growth hormone gene cluster to 17q22-24.

Authors:  M E Harper; H A Barrera-Saldaña; G F Saunders
Journal:  Am J Hum Genet       Date:  1982-03       Impact factor: 11.025

6.  Localization of a unique gene by direct hybridization in situ.

Authors:  D S Gerhard; E S Kawasaki; F C Bancroft; P Szabo
Journal:  Proc Natl Acad Sci U S A       Date:  1981-06       Impact factor: 11.205

7.  X-linked mental retardation with the fragile X. A study of 15 families.

Authors:  J F Mattei; M G Mattei; C Aumeras; M Auger; F Giraud
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.

Authors:  J Fishburn; G Turner; A Daniel; R Brookwell
Journal:  Am J Med Genet       Date:  1983-04

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.  Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry.

Authors:  K E Davies; B D Young; R G Elles; M E Hill; R Williamson
Journal:  Nature       Date:  1981-10-01       Impact factor: 49.962
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  18 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.

Authors:  M A Voelckel; N Philip; C Piquet; M C Pellissier; I Oberlé; F Birg; M G Mattei; J F Mattei
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

4.  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

5.  Repeated DNA sequences in the distal long arm of the human X chromosome.

Authors:  U Müller; U Tantravahi; A Monaco; H Stroh; L M Kunkel; S A Latt
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

6.  Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.

Authors:  R J Matthews; D S Anson; I R Peake; A L Bloom
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

7.  In situ hybridization studies using a molecular probe that maps to Xq27-Zq28.

Authors:  A M Duncan; C Morgan
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

8.  Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm.

Authors:  S H Roberts; M Upadhyaya; M Sarfarazi; P S Harper
Journal:  J Med Genet       Date:  1989-05       Impact factor: 6.318

9.  Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.

Authors:  C Schwartz; N Fitch; M C Phelan; C L Richer; R Stevenson
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

Review 10.  Recently recognized chromosomal defects of clinical importance.

Authors:  M Pembrey; M Baraitser
Journal:  Postgrad Med J       Date:  1986-02       Impact factor: 2.401
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