Prenatal diagnosis of mosaic complete trisomy 1q

American Journal of Medical Genetics, Part A

Volumn 149, Issue 8, 2009, Pages 1801-1805

  Schmitt, Colleen L ^a   Moldenhauer, Julie S ^b   Wolfe, Honor ^a   Kaiser Rogers, Kathleen ^a   Powell, Cynthia M ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; APNEA; ARACHNODACTYLY; CASE REPORT; CAUSE OF DEATH; CHROMOSOME 1Q; CHROMOSOME ANALYSIS; CHROMOSOME IDENTIFICATION; CLINICAL EXAMINATION; CONTRACTURE; CRYPTORCHISM; CYANOSIS; FEEDING DISORDER; FEMALE; FETUS ECHOGRAPHY; GENETIC COUNSELING; HEART FAILURE; HUMAN; HYDROCEPHALUS; IRIS COLOBOMA; KARYOTYPE 46,XY; LETTER; MALE; MICROGNATHIA; MICROSTOMIA; MOSAICISM; NASOGASTRIC TUBE; NEWBORN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SCROTUM DISORDER; SURVIVAL TIME; TRISOMY; TRISOMY 1Q; VAGINAL DELIVERY;

BRAIN DISEASES; CHROMOSOMES, HUMAN, PAIR 1; FATAL OUTCOME; FEMALE; GESTATIONAL AGE; HAND DEFORMITIES, CONGENITAL; HUMANS; INFANT, NEWBORN; KARYOTYPING; MALE; MOSAICISM; PHENOTYPE; PREGNANCY; PRENATAL DIAGNOSIS; TRISOMY; YOUNG ADULT;

EID: 68049109323     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32986     Document Type: Letter

References (11)

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