Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome
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Data
2011-05-01
Autores
Vieira, Gustavo H.
Rodriguez, Jayson D.
Boy, Raquel
Paiva, Isaias Soares de
Dupont, Barbara R.
Moretti-Ferreira, Danilo
Srivastava, Anand K.
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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
Como citar
American Journal of Medical Genetics, Part A, v. 155, n. 5, p. 988-992, 2011.