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A three-generation family with terminal microdeletion involving 5p15.33–32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome

✍ Scribed by Elmakky, Amira; Carli, Diana; Lugli, Licia; Torelli, Paola; Guidi, Battista; Falcinelli, Cristina; Fini, Sergio; Ferrari, Fabrizio; Percesepe, Antonio


Book ID
122322267
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
854 KB
Volume
57
Category
Article
ISSN
1769-7212

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