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Isochromosome 18q with karyotype 46, XX, i(18q). Cytogenetics and pathology
Author(s) -
FrosterIskenius Ursula,
Coerdt Wiltrud,
Rehder Helga,
Schwinger E.
Publication year - 1984
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.1399-0004.1984.tb01102.x
Subject(s) - isochromosome , karyotype , monosomy , cytogenetics , biology , fetus , pathology , chromosome , genetics , medicine , pregnancy , gene
Cytogenetic and morphological findings of a 20‐gestational‐week‐old female fetus with karyotype 46, XX, i(18q) are reported. The fetus displayed clinical features resembling Edward's syndrome. No characteristic symptoms of monosomy 18p could be observed.