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   <subfield code="a">DNA polymorphism of the human complement component C7 gene in familial deficiencies</subfield>
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   <subfield code="c">[Eliecer Coto, Eduardo Martínez-Naves, Orlando Domínguez, Carlos López-Larrea]</subfield>
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   <subfield code="a">Summary: A C7 cDNA probe detecting a TaqI restriction fragment length polymorphism has been used to examine the segregation of the &quot;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 informative. The &quot;silent allele” is linked to different TaqI alleles in both families. This suggests that at least two different C7*Q0 alleles are present in our population. This paper gives a protocol for genetic studies of hereditary traits in which the C7 gene and other genes tightly linked to it are involved.</subfield>
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