๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Centric fission of chromosome No. 7 in three generations

โœ Scribed by Dietmar Janke


Publisher
Springer
Year
1982
Tongue
English
Weight
314 KB
Volume
60
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Centric fission of chromosome No. 4 in t
โœ Bruno Dallapiccola; Pierpaolo Mastroiacovo; Enrico Gandini ๐Ÿ“‚ Article ๐Ÿ“… 1976 ๐Ÿ› Springer ๐ŸŒ English โš– 323 KB

Centric fission of chromosome No. 4 was found in the healthy mother of two children with trisomy 4p. The two telocentrics derived are stable and show no evidence of fusing again. The 2:3 ratio of unbalanced offsprings born to the proposita indicates that, contrary to the evidence emerging from studi

Centric fission of chromosome 9 in a boy
โœ Concolino, D.; Cinti, R.; Moricca, M.; Andria, G.; Strisciuglio, P. ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 12 KB ๐Ÿ‘ 1 views

A centric fission of chromosome 9 was found in a boy with trisomy 9p resulting from a de novo del (9p) and a 9p isochromosome. The patient presented with clinical findings similar to those described in previously reported cases of trisomy 9p. The cytogenetic evaluation and the molecular analysis usi

Paracentric inversion of chromosome 19 i
โœ Phelan, Mary C. ;Schroer, Richard J. ;Krug, Ernest F. ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 256 KB

We observed a paracentric inversion of 19p in a 15-month-old white boy with developmental delay and mild facial anomalies. The inversion of 19p was also present in his phenotypically normal mother and maternal grandfather.

Interstitial deletion of chromosome 7 de
โœ Marina Seabright; George M. Lewis ๐Ÿ“‚ Article ๐Ÿ“… 1978 ๐Ÿ› Springer ๐ŸŒ English โš– 203 KB

Chromosome studies were carried out on three patients for the following reasons: (1) growth retardation and mental subnormality in a boy; (2) marked developmental delay in a female infant; (3) routine check on a man whose wife had a stillborn with congenital anomalies. An interstitial deletion at 7q