Prenatal diagnosis of mitochondrial fatty acid oxidation defects

Prenatal Diagnosis

Volumn 16, Issue 2, 1996, Pages 117-124

  Nada, Mohamed A ^a   Vianey Saban, Christine ^b   Roe, Charles R ^a   Ding, Jia Huan ^a   Mathieu, Monique ^b   Wappner, Rebecca S ^c   Bialer, Martin G ^d   Mcglynn, Julie A ^d   Mandon, Ginette ^b  

^a BAYLOR UNIVERSITY MEDICAL CENTER   (United States)

^b HÔPITAL DEBROUSSE   (France)

^c INDIANA UNIVERSITY   (United States)

^d NORTH SHORE UNIVERSITY HOSPITAL   (United States)

Author keywords

Acylcarnitines; MCAD; Prenatal diagnosis; VLCAD

Indexed keywords

MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE;

AMNION CELL; ARTICLE; BLOOD ANALYSIS; CASE REPORT; CONTROLLED STUDY; DNA DETERMINATION; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FETUS; HUMAN; HUMAN CELL; ISOTOPE LABELING; LIPID METABOLISM; MASS SPECTROMETRY; METABOLIC DISORDER; MUTATION; PRENATAL SCREENING; PRIORITY JOURNAL;

ACYL-COA DEHYDROGENASE; ACYL-COA DEHYDROGENASE, LONG-CHAIN; AMNIOCENTESIS; CARBOXYLIC ESTER HYDROLASES; FEMALE; GESTATIONAL AGE; HUMANS; INFANT, NEWBORN; LIPID METABOLISM, INBORN ERRORS; MALE; MASS SPECTROMETRY; MITOCHONDRIA; OXIDATION-REDUCTION; PREGNANCY;

EID: 0030059946     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199602)16:2<117::AID-PD820>3.0.CO;2-Z     Document Type: Article

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