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A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome

✍ Scribed by Kobayashi, H.; Kasahara, M.; Hino, M.; Yoshimura, H.; Takahara, S.; Ikeda, K.; Son, C.; Iwakura, T.; Yoshimoto, A.; Ishihara, T.; Ogawa, Y.

Book ID: 125337250
Publisher: Springer-Verlag
Year: 2006
Tongue: English
Weight: 92 KB
Volume: 29
Category: Article
ISSN: 0391-4097
DOI: 10.1007/BF03347383

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TABLE I. Colony-Forming Assay From CD34 + Bone Marrow Cells Serum a BFU-E/10 2 CD34 + cells Control 1 50.2 ± 4.6 Control 2 48.5 ± 14.1 Before chemotherapy 24.4 ± 6.2 b After chemotherapy 50.5 ± 6.5 Values are means ± SD of triplicate cultures. a Control 1; normal AB serum, Control 2; serum from a pa