Literature DB >> 4548443

New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.

M Zatz, S B Itskan, R Sanger, O Frota-Pessoa, P H Saldanha.   

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Year:  1974        PMID： 4548443      PMCID： PMC1013198          DOI： 10.1136/jmg.11.4.321

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


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  14 in total

1.  GLUCOSE-6-PHOSPHATE DEHYDROGENASE, COLOUR VISION AND XG BLOOD GROUPS IN GREECE: LINKAGE AND POPULATION DATA.

Authors:  G R FRASER; B DEFARANAS; C A KATTAMIS; R R RACE; R SANGER; G STAMATOYANNOPOULOS
Journal:  Ann Hum Genet       Date:  1964-06       Impact factor: 1.670

2.  Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and colour-blindness in American Negroes.

Authors:  I H PORTER; J SCHULZE; V A MCKUSICK
Journal:  Ann Hum Genet       Date:  1962-11       Impact factor: 1.670

3.  Colour blindness and the Duchenne-type muscular dystrophy.

Authors:  U PHILIP; C A SMITH; J N WALTON
Journal:  Ann Hum Genet       Date:  1956-11       Impact factor: 1.670

4.  [Genetics of myopathy].

Authors:  P E BECKER
Journal:  Dtsch Z Nervenheilkd       Date:  1955

5.  Sequential tests for the detection of linkage.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1955-09       Impact factor: 11.025

6.  The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups.

Authors:  A E Emery; C A Smith; R Sanger
Journal:  Ann Hum Genet       Date:  1969-01       Impact factor: 1.670

7.  Carrier detection in X-linked muscular dystrophy.

Authors:  J N Walton
Journal:  J Genet Hum       Date:  1969-10

8.  A comparison of the two-generation and three-generation methods of estimating linkage values on the X chromosome in man with special reference to the loci determining the Xg blood group and glucose-6-phosphate dehydrogenase deficiency.

Authors:  G R Fraser; O Mayo
Journal:  Am J Hum Genet       Date:  1968-11       Impact factor: 11.025

9.  [A benign X-chromosomal hereditary muscular dystrophy. I. Examinations of symptom-carriers].

Authors:  H W Rotthauwe; S Kowalewski
Journal:  Humangenetik       Date:  1966

10.  The Genetics of Angiokeratoma Corporis Diffusum (Fabry's Disease) and Its Linkage Relations with the Xg Locus.

Authors:  J M Opitz; F C Stiles; D Wise; R R Race; R Sanger; G R Von Gemmingen; R R Kierland; E G Cross; W P De Groot
Journal:  Am J Hum Genet       Date:  1965-07       Impact factor: 11.025
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  13 in total

1.  A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information.

Authors:  M Sarfarazi; H Williams
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

2.  Ultrastructural studies on the neuromuscular junctions of Becker's muscular dystrophy.

Authors:  N Fukuhara; M Suzuki; T Tsubaki; S Kushiro; N Takasawa
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

3.  X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg.

Authors:  M Zatz; C Penha-Serrano; P A Otto
Journal:  J Med Genet       Date:  1976-06       Impact factor: 6.318

4.  Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.

Authors:  L Roncuzzi; S Fadda; M Mochi; L Prosperi; S Sangiorgi; R Santamaria; D Sbarra; D Besana; L Morandi; M Rocchi
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

5.  Some recent developments in psychiatric genetics.

Authors:  J Shields
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1975-12-22

6.  Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences.

Authors:  H M Kingston; M Sarfarazi; N S Thomas; P S Harper
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.

Authors:  M Zatz; A M Vianna-Morgante; P Campos; A J Diament
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

8.  Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy.

Authors:  D E Wilcox; N A Affara; J R Yates; M A Ferguson-Smith; P L Pearson
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

9.  Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.

Authors:  H M Kingston; N S Thomas; P L Pearson; M Sarfarazi; P S Harper
Journal:  J Med Genet       Date:  1983-08       Impact factor: 6.318

10.  Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9).

Authors:  S Fadda; M Mochi; L Roncuzzi; S Sangiorgi; D Sbarra; M Zatz; G Romeo
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132
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