𝔖 Bobbio Scriptorium
✦   LIBER   ✦

CD4 deficiency in myelodysplastic syndrome with monosomy 7

✍ Scribed by C. M. R. Weemaes; F. Preijers; G. A. M. de Vaan; J. A. J. M. Bakkeren; I. S. Klasen; A. Haraldsson


Publisher
Springer
Year
1996
Tongue
English
Weight
237 KB
Volume
155
Category
Article
ISSN
0340-6997

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Loss of maternal allele in a child with
✍ Aktas, Dilek; Yenicesu, Id?l; H?csonmez, Gonul; Tuncbilek, Ergul πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 72 KB πŸ‘ 2 views

Monosomy 7 or partial deletion of the long arm of chromosome 7 is frequently described in children with myelodysplastic syndrome and acute myeloblastic leukemia. Parental origin of chromosome 7 in children with sporadic monosomy 7 has been examined very rarely. To investigate if monosomy 7 shows par

Better prognosis for patients with del(7
✍ Iris Cordoba; JosΓ© R. GonzΓ‘lez-Porras; Benet Nomdedeu; Elisa LuΓ±o; Raquel de Paz πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 292 KB

## Abstract ## BACKGROUND: Abnormalities involving chromosome 7 are frequent in myelodysplastic syndrome (MDS) and suggest a poor prognosis. ## METHODS: The authors examined the hypothesis that the clinical features and survival associated with isolated deletion (del) of part of the long arm of

Monosomy 7 myelodysplastic syndrome and
✍ John M. Maris; Susan R. Wiersma; Nidal Mahgoub; Patricia Thompson; Russell J. Ge πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 126 KB πŸ‘ 2 views

## Background: Children with neurofibromatosis type 1 (nf1) are at increased risk of developing benign and malignant solid tumors as well as hematologic malignancies, including de novo juvenile chronic myelogenous leukemia, monosomy 7 syndrome, and acute myelogenous leukemia. the normal nf1 allele

Familial sideroblastic anemia with emerg
✍ Kardos, G.; Veerman, A.J.P.; de Waal, F.C.; van Oudheusden, L.J.; Slater, R. πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 356 KB πŸ‘ 1 views

The case history of two sisters with pyridoxine-refractory familial sideroblastic anemia (FSA) is presented in which one developed a myelodysplastic syndrome (MDS) with monosomy for chromosome 5. Bone marrow examination of both patients at diagnosis showed erythroid hyperplasia with more than 50% ri