Delección distal 4p16: síndrome de Wolf-Hirschhorn
Gayol, Luís; Quiñones, Olga; Menéndez, Ibis; Guerra, Rosa.
Rev. cuba. pediatr
; 60(3): 423-30, mayo-jun. 1988. ilus, tab
Artículo en Español | CUMED | ID: cum-4571
Documentos relacionados
Concomitant deletion of the short arm (del(1p13.3)) and amplification or gain (1q21) of chromosome 1 by fluorescence in situ hybridization are associated with a poor clinical outcome in multiple myeloma.
Making a case for del(1p) as a high-risk abnormality in multiple myeloma.
Parallel deletion and duplication at 7q11.23 in a silent carrier for two reciprocal syndromic disorders.
Engineering large-scale chromosomal deletions by CRISPR-Cas9.
[Genetic analysis of a family with 9q34.3 microdeletion and microduplication caused by abnormal chromosome balance structure].
Unusual neuroimaging features in a patient with chromosome 11q14.1-11q23.2 deletion.
[Prenatal diagnosis of a fetus with 8q13.3 microdeletion through chromosomal microarray analysis].
del(1p32), a powerful prognostic factor in myeloma.
Patterns of Chromosomal Aberrations in Solid Tumors.
[Analysis of chromosome in 1 324 patients with oligozoospermia or azoosperm].