Precise prenatal diagnosis of tuberous sclerosis by sequencing the TSC2 gene

Prenatal Diagnosis

Volumn 25, Issue 7, 2005, Pages 582-585

  Milunsky, Aubrey ^a   Shim, Sung Han ^a   Ito, Masamichi ^a   Jaekle, Ronald K ^b   Bassett, Lori L ^b   Brumund, Michael R ^c   Milunsky, Jeff M ^a  

^a BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WOMAN S HOSPITAL   (United States)

^c Pediatric Cardiology Associates   (United States)

Author keywords

Gene mutation; Prenatal diagnosis; Rhabdomyoma; Tuberous sclerosis

Indexed keywords

ADULT; AMNIOTIC FLUID CELL; ARTICLE; CASE REPORT; DIAGNOSTIC KIT; DIAGNOSTIC PROCEDURE; DNA EXTRACTION; FEMALE; FETUS; GENE; GENE MUTATION; GENE SEQUENCE; HEART TUMOR; HUMAN; MOLECULAR CLONING; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TSC1 GENE; TSC2 GENE; TUBEROUS SCLEROSIS;

ADULT; AMNIOCENTESIS; DIAGNOSIS, DIFFERENTIAL; FEMALE; GENES, TUMOR SUPPRESSOR; HUMANS; INFANT, NEWBORN; MUTATION; PREGNANCY; PREGNANCY TRIMESTER, SECOND; PRENATAL DIAGNOSIS; TUBEROUS SCLEROSIS; TUMOR SUPPRESSOR PROTEINS;

EID: 23244446012     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1197     Document Type: Article

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