𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Terminal deletion of the short arm of chromosome 3

✍ Scribed by Masami Asai; Yasuhiko Ito; Toshiyuki Iguchi; Jin Ito; Noboru Okada; Hidetsune Oishi


Publisher
Nature Publishing Group
Year
1992
Tongue
English
Weight
973 KB
Volume
37
Category
Article
ISSN
1435-232X

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Interstitial deletion of the short arm o
✍ J. M. Hertz; W. Coerdt; N. Hahnemann; M. Schwartz πŸ“‚ Article πŸ“… 1988 πŸ› Springer 🌐 English βš– 248 KB

A de novo interstitial deletion of the short arm of chromosome 3 was prenatally diagnosed in a male fetus, karyotype 46,XY,del(3)(pter----p14.2::p11----qter). The fetus had craniofacial dysmorphisms, a single transverse palmar crease, ulnar deviation in the wrists, cardiovascular anomalies, a slight

Short arm deletion of chromosome 12
✍ E. Orye; M. Craen πŸ“‚ Article πŸ“… 1975 πŸ› Springer 🌐 English βš– 1004 KB

Two boys (W.M. and C.P.) are described, in each of whom a short-arm deleted C chromosome was apparently present. The clinical findings on W.M. are stenosis of the sagittal sutura associated with atrophy of the nervus opticus and mental retardation, and on C.P. osteogenesis imperfecta. An analysis of

Deletion of the short arm of chromosome
✍ J. P. Fryns; J. C. Pedersen; H. Duyck; G. Fabry; H. Berghe πŸ“‚ Article πŸ“… 1980 πŸ› Springer 🌐 English βš– 755 KB
Deletion of the short arm of chromosome
✍ Nikos Pandis; Georgia Bardi; Felix Mitelman; Sverre Helm πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 61 KB πŸ‘ 3 views

Deletions in the short arm of chromosome 3 have long been known to be common in many tumor types, including carcinomas of the lung and kidney. Small interstitial deletions of the proximal-central region of 3p, with band 3p14 as a minimal common deleted segment, have recently been shown to occur in a

Deletion of the short arms of chromosome
✍ Dagmar K. Kalousek; Serge ThΓ©rien πŸ“‚ Article πŸ“… 1976 πŸ› Springer 🌐 English βš– 440 KB

A 46, XX, del(20) (p11) karyotype (Paris Conference, 1971) was identified in an 11-month-old French-Canadian girl with a dysmorphic syndrome, multiple congenital anomalies, psychomotor and growth retardation. Both parents had normal phenotype and karyotype.