Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization

Prenatal Diagnosis

Volumn 27, Issue 4, 2007, Pages 373-379

  Cain, Colyn Cargile ^a   Saul, Daniel ^a   Attanasio, Lisa ^a   Oehler, Erin ^a   Hamosh, Ada ^a   Blakemore, Karin ^a   Stetten, Gail ^a,b  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b DEPARTMENT OF PATHOLOGY   (United States)

Author keywords

Array CGH; FISH; MLS syndrome; X; Y translocation

Indexed keywords

ADULT; AMNION CELL; ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART MALFORMATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HYGROMA; INTRAUTERINE GROWTH RETARDATION; KARYOTYPING; LYMPHOBLAST; MICROPHTHALMIA; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SKIN DEFECT; X CHROMOSOME; Y CHROMOSOME;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOMES, HUMAN, X; FATAL OUTCOME; FEMALE; HUMANS; HYBRIDIZATION, GENETIC; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MICROPHTHALMOS; PREGNANCY; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATIONS; SKIN ABNORMALITIES; SYNDROME; ULTRASONOGRAPHY, PRENATAL;

EID: 34247144490     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1674     Document Type: Article

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