ArrayCGH characterization of a deletion on 2q13 associated with developmental delay and facial dysmorphism (case report)

• Authors: SLÁMOVÁ Iva; ZRNOVÁ HLADÍLKOVÁ Eva; BAROY Tuva; VALLOVÁ Vladimíra; PRÁŠILOVÁ Šárka; GAILLYOVÁ Renata; FRENGEN E; KUGLÍK Petr
• Year of publication: 2012
• Type: Conference abstract