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P44.08: Case report of a complete trisomy 9

✍ Scribed by N. N. Martins; H. R. Gaspar; M. R. Pinto; C. Barbedo; M. S. Gomes; M. H. Pereira

Book ID
112226740
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
38 KB
Volume
30
Category
Article
ISSN
0960-7692

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πŸ“œ SIMILAR VOLUMES

Complete trisomy 9 in a term fetus: A ca
Complete trisomy 9 in a term fetus: A case report
✍ Daniel Roshanfekr; Cecilia Dahl-Lyons; Eva Pressman; Serdar Ural; Karin Blakemor πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 102 KB πŸ‘ 2 views

Complete trisomy 9 was diagnosed in a 35-week fetus by amniocentesis. Several sonograms had revealed only a two-vessel cord and intrauterine growth restriction. No other abnormalities were noted. A stillborn infant was delivered at 37 weeks gestation after induction of labor.

Partial and complete trisomy 9: Delineat
Partial and complete trisomy 9: Delineation of a trisomy 9 syndrome
✍ Grant R. Sutherland; Rodney F. Carter; Lloyd L. Morris πŸ“‚ Article πŸ“… 1976 πŸ› Springer 🌐 English βš– 940 KB

Two infants with trisomy involving chromosome 9 are described. One had complete trisomy 9 and the other karyotype 47,XX,+der(9),t(7;9) (p22;q32)mat. A trisomy 9 syndrome is delineated, consisting of features of the trisomy 9p syndrome and various other malformations. These include abnormalities of t

Possible intrachromosomal duplication in
Possible intrachromosomal duplication in a case of trisomy 9p
✍ H. Chiyo; J. Furuyama; N. Suehara; Y. Obashi; H. Kikkawa; F. Ikoma πŸ“‚ Article πŸ“… 1976 πŸ› Springer 🌐 English βš– 588 KB

A 5-year-old boy with multiple minor anomalies and mental retardation was found to have chromosomal condition of 46,XY,inv dup(9p) (pter leads to p13::p21 leads to p24::p13 leads to qter). The clinical features of the propositus fit well with those of trisomy 9p which have been established to be a c