Vivarelli R, Scarinci R, Conti G, Anichini C
Pediatr Med Chir. 1985 May-Jun;7(3):451-3.
We refer about two children with Wolf-Hirschhorn's syndrome or syndrome with partial deletion of short arm of chromosome number 4. The diagnosis was possible with an accurate estimation of phenotype. Cytogenetics examination showed the chromosomal aberration typical for this syndrome.
我们报告了两名患有沃尔夫-赫希霍恩综合征或4号染色体短臂部分缺失综合征的儿童。通过对表型的准确评估得以确诊。细胞遗传学检查显示出该综合征典型的染色体畸变。