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Polymerase chain reaction (PCR) for detection of MspI polymorphism at the D3S2 locus.

作者信息

Ganly P S, Rabbitts P H

机构信息

Medical Research Council Clinical Oncology and Radiotherapeutics Unit, Medical Research Council Centre, Cambridge, UK.

出版信息

Nucleic Acids Res. 1991 Jul 11;19(13):3761.

PMID:1712946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC328435/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bea/328435/23efe25e4556/nar00093-0270-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bea/328435/ddb559f59335/nar00093-0270-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bea/328435/23efe25e4556/nar00093-0270-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bea/328435/ddb559f59335/nar00093-0270-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bea/328435/23efe25e4556/nar00093-0270-b.jpg

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引用本文的文献

1
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosa.VII型胶原蛋白基因（COL7A1）标记物在隐性营养不良型大疱性表皮松解症产前诊断中的应用。
J Med Genet. 1995 Sep;32(9):749-50. doi: 10.1136/jmg.32.9.749.
2
Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus.三个英国家庭中常染色体显性营养不良性大疱性表皮松解症与靠近COL7A1基因座的标记D3S2的连锁关系。
J Med Genet. 1992 Jun;29(6):381-2. doi: 10.1136/jmg.29.6.381.

本文引用的文献

1
Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13).
Genomics. 1989 May;4(4):518-29. doi: 10.1016/0888-7543(89)90275-9.
2
Identification of two human ferritin H genes on the short arm of chromosome 6.
Genomics. 1990 Feb;6(2):204-11. doi: 10.1016/0888-7543(90)90558-c.