Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia

American Journal of Medical Genetics, Part A

Volumn 152, Issue 1, 2010, Pages 102-110

  D'Angelo, Carla S ^a   Kohl, Ilana ^a   Varela, Monica Castro ^a   De Castro, Cláudia I E ^a   Kim, Chong A ^a   Bertola, Débora R ^a   Lourenço, Charles M ^a   Koiffmann, Cȩlia P ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Hyperphagia; MLPA; Monosomy 1p36; Obesity

Indexed keywords

GENOMIC DNA;

ADOLESCENT; ADULT; ARTICLE; BODY MASS; CHILD; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME IDENTIFICATION; CHROMOSOME MAP; CHROMOSOME REARRANGEMENT; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; DNA EXTRACTION; FEMALE; GENE AMPLIFICATION; GENE DELETION; GENETIC ASSOCIATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPERPHAGIA; MAJOR CLINICAL STUDY; MALE; MONOSOMY 1P36 SYNDROME; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; OBESITY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; CHROMOSOME 1P; GENE FREQUENCY; GENE SEQUENCE; GENETIC POLYMORPHISM; INFANT; MONOSOMY; MONOSOMY 1P36; SEQUENCE ANALYSIS;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; COHORT STUDIES; HUMANS; HYPERPHAGIA; IN SITU HYBRIDIZATION, FLUORESCENCE; OBESITY; PHENOTYPE;

EID: 75149120622     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33160     Document Type: Article

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