Prenatal identification of a heterozygous status in two fetuses at risk for glucose-galactose malabsorption

Prenatal Diagnosis

Volumn 16, Issue 5, 1996, Pages 458-462

  Martín, Martín G ^a   Turk, Eric ^a   Kerner, Cynthia ^a   Zabel, Bernard ^b   Wirth, Stefan ^b   Wright, Ernest M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

Autosomal recessive; Diarrhoea; SGLT1; Sugar transport

Indexed keywords

GALACTOSE; GLUCOSE;

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; DIARRHEA; FETUS; GLUCOSE METABOLISM; HUMAN; INBORN ERROR OF METABOLISM; MALABSORPTION; MISSENSE MUTATION; MOLECULAR BIOLOGY; POLYMERASE CHAIN REACTION; PRENATAL SCREENING; PRIORITY JOURNAL; SUGAR TRANSPORT;

AMNIOCENTESIS; BREATH TESTS; CONSANGUINITY; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; DIARRHEA; DNA; DNA PRIMERS; FEMALE; FETAL DISEASES; GALACTOSE; GLUCOSE; HETEROZYGOTE DETECTION; HUMANS; MALABSORPTION SYNDROMES; MEMBRANE GLYCOPROTEINS; MONOSACCHARIDE TRANSPORT PROTEINS; PEDIGREE; POLYMERASE CHAIN REACTION; PREGNANCY; REAGENT KITS, DIAGNOSTIC; RESTRICTION MAPPING; RISK FACTORS; SODIUM-GLUCOSE TRANSPORTER 1;

EID: 0029927304     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199605)16:5<458::AID-PD873>3.0.CO;2-U     Document Type: Article

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