良性（贝克型）X连锁肌营养不良症、色盲和Xg血型基因座的连锁关系。 - Suppr

Suppr

超能文献

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

作者信息

Emery A E, Smith C A, Sanger R

出版信息

Ann Hum Genet. 1969 Jan;32(3):261-9. doi: 10.1111/j.1469-1809.1969.tb00075.x.

DOI:10.1111/j.1469-1809.1969.tb00075.x

PMID:5305175

Abstract

摘要

相似文献

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

Ann Hum Genet. 1969 Jan;32(3):261-9. doi: 10.1111/j.1469-1809.1969.tb00075.x.

Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness.

J Med Genet. 1974 Dec;11(4):317-20. doi: 10.1136/jmg.11.4.317.

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

J Med Genet. 1974 Dec;11(4):321-7. doi: 10.1136/jmg.11.4.321.

Family in which Duchenne's muscular dystrophy and protan colour blindness are segregating.

J Med Genet. 1977 Apr;14(2):130-2. doi: 10.1136/jmg.14.2.130.

The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.

J Med Genet. 1975 Jun;12(2):131-4. doi: 10.1136/jmg.12.2.131.

Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.

J Med Genet. 1966 Jun;3(2):92-5. doi: 10.1136/jmg.3.2.92.

X-linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred.

Ann Hum Genet. 1969 May;32(4):333-45. doi: 10.1111/j.1469-1809.1969.tb00084.x.

Linkage relations of X-borne ichthyosis to the Xg blood groups and to other markers of the X in Israelis.

Ann Hum Genet. 1969 May;32(4):323-32. doi: 10.1111/j.1469-1809.1969.tb00082.x.

The linkage between Duchenne-type progressive muscular dystrophy and color blindness.

Pol Med J. 1970;9(5):1207-11.

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

Hum Genet. 1984;67(1):6-17. doi: 10.1007/BF00270551.

引用本文的文献

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

J Med Genet. 1983 Aug;20(4):255-8. doi: 10.1136/jmg.20.4.255.

Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.

Hum Genet. 1984;66(1):17-40. doi: 10.1007/BF00275183.

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.

Am J Hum Genet. 1984 Mar;36(2):265-76.

Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy.

Hum Genet. 1983;65(2):169-71. doi: 10.1007/BF00286656.

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

Hum Genet. 1984;67(1):6-17. doi: 10.1007/BF00270551.

Hypoxanthine-guanine phosphoribosyltransferase deficiency and Xg blood group.

Am J Hum Genet. 1970 Jan;22(1):50-4.

Abnormalities of the electrocardiogram in hereditary myopathies.

J Med Genet. 1972 Mar;9(1):8-12. doi: 10.1136/jmg.9.1.8.

[New data on the genetics and classification of muscular dystrophies].

Humangenetik. 1972;17(1):1-22.

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

J Med Genet. 1974 Dec;11(4):321-7. doi: 10.1136/jmg.11.4.321.

Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness.

J Med Genet. 1974 Dec;11(4):317-20. doi: 10.1136/jmg.11.4.317.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验