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pro vyhledávání: '"Oksana Ivanovna Ritenkova"'
Publikováno v:
Journal of obstetrics and women's diseases. 64:106-109
We discuss the case of a family carriers of structural chromosomal aberration del(6)(q24) in two generations. For the first time revealed in 2 year old girl, the aberration has become a reason for family medical and genetic examination, including pre