Literature DB >> 5298508

Christmas disease, color-blindness and blood group Xga.

R L Wall, J McConnell, D Moore, C R Macpherson, A Marson.   

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Year:  1967        PMID： 5298508     DOI： 10.1016/0002-9343(67)90166-0

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  7 in total

1.  Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).

Authors:  K E Davies; M G Mattei; J F Mattei; H Veenema; S McGlade; K Harper; N Tommerup; K B Nielsen; M Mikkelsen; P Beighton
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  Consanguinity and blood group distribution in an Amish Isolate.

Authors:  C E Jackson; W E Symon; E L Pruden; I M Kaehr; J D Mann
Journal:  Am J Hum Genet       Date:  1968-11       Impact factor: 11.025

3.  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

4.  Low cancer incidence rates in Ohio Amish.

Authors:  Judith A Westman; Amy K Ferketich; Ross M Kauffman; Steven N MacEachern; J R Wilkins; Patricia P Wilcox; Robert T Pilarski; Rebecca Nagy; Stanley Lemeshow; Albert de la Chapelle; Clara D Bloomfield
Journal:  Cancer Causes Control       Date:  2009-09-25       Impact factor: 2.506

5.  T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detection.

Authors:  R P Ketterling; C D Bottema; D D Koeberl; S Ii; S S Sommer
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

6.  Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site.

Authors:  P Szabo; M Purrello; M Rocchi; N Archidiacono; B Alhadeff; G Filippi; D Toniolo; G Martini; L Luzzatto; M Siniscalco
Journal:  Proc Natl Acad Sci U S A       Date:  1984-12       Impact factor: 11.205

7.  The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

Authors:  M Purrello; B Alhadeff; D Esposito; P Szabo; M Rocchi; M Truett; F Masiarz; M Siniscalco
Journal:  EMBO J       Date:  1985-03       Impact factor: 11.598
  7 in total

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