DNA polymorphism of the human complement
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Eliecer Coto; Eduardo MartΓnez-Naves; Orlando DomΓnguez; Carlos LΓ³pez-Larrea
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Article
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1990
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Springer
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English
β 207 KB
A C7 cDNA probe detecting a TaqI restriction fragment length polymorphism has been used to examine the segregation of the "silent allele" (C7\*Q0) in two familial deficiencies. Carrier diagnosis in healthy children is possible when both parents are heterozygotes. Only one of these two families was i