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Paracentric inversions in man
Author(s) -
Callen D. F.,
Woollatt E.,
Sutherland G. R.
Publication year - 1985
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1985.tb01224.x
Subject(s) - chromosomal inversion , genetics , prenatal diagnosis , biology , karyotype , pregnancy , gene , chromosome , fetus
Two new cases of familial paracentric inversions, 46, XY, inv(3)(p21.1p25) and 46, XY, inv(7) (q22.3q36.1) are presented. A review of published cases suggests that prenatal diagnosis for carriers of paracentric inversions is not warranted. However, care must be exercised in eliminating the possibility of insertions.

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