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FŒTAL HÆMOGLOBIN AND NEUTROPHIL ANOMALY IN THE D1-TRISOMY SYNDROME

✍ Scribed by Powars, Darlene; Rohde, Russell; Graves, Doris


Book ID
122048720
Publisher
The Lancet
Year
1964
Tongue
English
Weight
426 KB
Volume
283
Category
Article
ISSN
0140-6736

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A case of an inherited type of D/G translocation D1-trisomy syndrome was described. A female proposita who had the clinical signs of D1-trisomy syndrome was found to have a chromosome complement of 46,XX,--G,+t(DqGq). examination of Q- and G-stained karyotypes revealed that the chromosomes involved