Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome - Vieira, Gustavo H.; Rodriguez, Jayson D.; Boy, Raquel; Paiva, Isaias Soares de; Dupont, Barbara R.; Moretti-Ferreira, Danilo; Srivastava, Anand K. (Wiley, 2011)
Keywords: 1p36 deletion syndrome; adolescent; behavior disorder; case report; chromosome deletion; clinical feature; comparative genomic hybridization; craniofacial malformation; differential diagnosis; female; genotype; human; intellectual impairment; letter; muscle hypotonia; priority journal; seizure; single nucleotide polymorphism; sleep disorder; Smith Magenis syndrome; speech disorder; Adolescent; Chromosome Deletion; Chromosomes, Human, Pair 1; Diagnosis, Differential; Female; Humans; Smith-Magenis Syndrome; Syndrome