Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q
Journal Article
·
· American Journal of Medical Genetics
- Univ. of Sao Paulo (Brazil); and others
Deletion 11q23{r_arrow}qter and duplication 12q23{r_arrow}qter are described in a boy with neuroblastoma, multiple congenital anomalies, and mental retardation. The patient has clinical manifestations of 11q deletion and 12q duplication syndromes. The possible involvement of the segment 11q23{r_arrow}24 in the cause of the neuroblastoma is discussed. 18 refs., 2 figs., 1 tab.
- Sponsoring Organization:
- USDOE
- OSTI ID:
- 441152
- Journal Information:
- American Journal of Medical Genetics, Vol. 58, Issue 1; Other Information: PBD: 31 Jul 1995
- Country of Publication:
- United States
- Language:
- English
Similar Records
Study of two patients with craniosynostosis and deletions of 11q: One with features of Saethre-Chotzen syndrome and the other with concomitant partial trisomy 4q
The distal 8p deletion (8)(p23.1): A common syndrome associated with cogenital heart defect and mental retardation?
Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization
Journal Article
·
Thu Sep 01 00:00:00 EDT 1994
· American Journal of Human Genetics
·
OSTI ID:441152
The distal 8p deletion (8)(p23.1): A common syndrome associated with cogenital heart defect and mental retardation?
Journal Article
·
Thu Sep 01 00:00:00 EDT 1994
· American Journal of Human Genetics
·
OSTI ID:441152
Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization
Journal Article
·
Mon Sep 11 00:00:00 EDT 1995
· American Journal of Medical Genetics
·
OSTI ID:441152
+1 more