Ring chromosome 13 in an infant with multiple congenital anomalies and penoscrotal transposition
1998 ◽
Vol 7
(4)
◽
pp. 299-301
◽
2012 ◽
Vol 27
(8)
◽
pp. 948
◽
Keyword(s):
Deletion (13)(q22) with multiple congenital anomalies, hydranencephaly and penoscrotal transposition
1996 ◽
Vol 5
(4)
◽
pp. 289???294
◽
1990 ◽
Vol 27
(7)
◽
pp. 462-464
◽
1995 ◽
Vol 57
(3)
◽
pp. 494-495
◽
2021 ◽
Vol 60
(4)
◽
pp. 771-774