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Autor:
Zong-Qi Dai, Jérôme Toutain, Didier Lacombe, Fanny Morice-Picard, Laurence Taine, Jacques Horovitz, Robert Saura, Benoit Arveiler, Houria Hallal
Publikováno v:
European Journal of Medical Genetics. 54:292-294
We report an unusual chromosome 22q11 deletion associated with an apparent complementary ring chromosome in a phenotypically normal woman with a family medical history of 22q11 deletion. Using peripheral blood samples, conventional karyotyping, Fluor