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The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromes

✍ Scribed by Robert S. Young; Terry Reed; M. E. Hodes; Catherine G. Palmer

Publisher
Springer
Year
1982
Tongue
English
Weight
827 KB
Volume
62
Category
Article
ISSN
0340-6717

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A low-birth-weight near-term male infant was found to have a non-familial 47,XΒ₯ chromosome complement with an extra medimn-sized metacentrie chromosome slightly larger than a number 16. By Giemsa-trypsin (G-banding) this extra chromosome was determined to be a number 9 with deletion of approximately

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