De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2

American Journal of Medical Genetics, Part A

Volumn 161, Issue 4, 2013, Pages 894-896

  Tassano, E ^a   Di Rocco, M ^a   Signa, S ^a   Gimelli, G ^a  

^a G GASLINI INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

MICRORNA; MICRORNA 17; MICRORNA 92; UNCLASSIFIED DRUG;

CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME DELETION 13Q31; CHROMOSOME DELETION 13Q32; FACE DYSMORPHIA; FEINGOLD SYNDROME 2; FEMALE; FOOT MALFORMATION; GENETIC DISORDER; GROWTH DISORDER; GROWTH RETARDATION; HAND MALFORMATION; HUMAN; INTERSTITIAL CHROMOSOME DELETION; KARYOTYPE; LETTER; MICROCEPHALY; MUSCLE HYPOTONIA; NEUROLOGIC EXAMINATION; PHYSICAL EXAMINATION; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 13; COMPARATIVE GENOMIC HYBRIDIZATION; EYELIDS; FEMALE; HUMANS; INFANT; INTELLECTUAL DISABILITY; LIMB DEFORMITIES, CONGENITAL; MICROCEPHALY; MICRORNAS; MULTIGENE FAMILY; PHENOTYPE; TRACHEOESOPHAGEAL FISTULA;

EID: 84875495957     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.35781     Document Type: Letter

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