𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Erythroleukemia in a child associated with monosomy 7

✍ Scribed by Toshiji Shitara; Shin-Ichiroh Yugami; Manabu Sotomatu; Yukio Oshima; Hiroko Ijima; Takayoshi Kuroume


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
266 KB
Volume
68
Category
Article
ISSN
0008-543X

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

Full mosaic monosomy 22 in a child with
✍ Pinto-Escalante, Doris; Ceballos-Quintal, Jose M.; Castillo-Zapata, Ileana; Cant πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 24 KB πŸ‘ 2 views

We describe an abnormal premature male infant with mosaic monosomy of chromosome 22. He had a unique facial appearance, similar to those with DiGeorge syndrome, and hypertonicity, limitation of extension at major joints, and flexion contractures of all fingers. This rare chromosomal aberration has b

Developmental profile in a patient with
✍ Pellegrino, Joan E.; Pellegrino, Louis; Spinner, Nancy B.; Sladky, John; Chance, πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 22 KB πŸ‘ 1 views

We report on a patient with dup(l7p) and monosomy (1Oq) resulting from a familial translocation. Manifestations typical of both syndromes were present. The overall development of this patient was better by comparison with similar reported cases of either anomaly. Our evaluation detected severe gross