Microdeletion of 16p11.2 associated with endocardial fibroelastosis

American Journal of Medical Genetics, Part A

Volumn 152, Issue 9, 2010, Pages 2383-2386

  Puvabanditsin, Surasak ^a   Nagar, Michael S ^a   Joshi, Meera ^a   Lambert, George ^a   Garrow, Eugene ^b   Brandsma, Erik ^a  

^a ROBERT WOOD JOHNSON MEDICAL SCHOOL   (United States)

^b Downstate Health Sciences University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARDIOMEGALY; CASE REPORT; CHROMOSOME 16P; COMPARATIVE GENOMIC HYBRIDIZATION; CONGESTIVE CARDIOMYOPATHY; ECHOCARDIOGRAPHY; ENDOCARDIAL FIBROELASTOSIS; FEMALE; FETUS; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GESTATIONAL AGE; HUMAN; LETTER; NEWBORN; PRIORITY JOURNAL; PULMONARY VALVE ATRESIA; THORAX RADIOGRAPHY;

AUTOPSY; CHROMOSOMES, HUMAN, PAIR 16; ENDOCARDIAL FIBROELASTOSIS; FAMILY; FATAL OUTCOME; HUMANS; INFANT, NEWBORN; MALE; SEQUENCE DELETION;

EID: 77956122632     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33562     Document Type: Letter

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