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Deletion of part of the short arm of chromosome 17 in a congenital fibrosarcoma

✍ Scribed by Patricia A. Gorman; Marian Malone; Jon Pritchard; Denise Sheer


Book ID
119104641
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
492 KB
Volume
48
Category
Article
ISSN
0165-4608

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A 46, XX, del(20) (p11) karyotype (Paris Conference, 1971) was identified in an 11-month-old French-Canadian girl with a dysmorphic syndrome, multiple congenital anomalies, psychomotor and growth retardation. Both parents had normal phenotype and karyotype.