✦ LIBER ✦

47,+(9q-) in unrelated three children with plasma growth hormon deficiency

✍ Scribed by Hiroko Fujita; Motoko Shimazaki; Toru Takeuchi; Yasushi Hayakawa; Toshiaki Oura

Book ID: 104695228
Publisher: Springer
Year: 1976
Tongue: English
Weight: 550 KB
Volume: 31
Category: Article
ISSN: 0340-6717
DOI: 10.1007/bf00270857

No coin nor oath required. For personal study only.

✦ Synopsis

Marker chromosomes carried by unrelated 3 cases were identified as a part of No. 9 chromosome through the analysis of the chromatid fine structure after trypsin-giemsa treatment. They showed characteristic features of that 9p trisomic syndrome which were described by Rethoré et al. (1973). In addition to those features, some clinical and laboratory findings on growth hormon deficiency were disclosed in this report.

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