Galactose-1-Phosphate Uridyl Transferase Deficiency Is Not Associated with Müllerian Aplasia in Dutch Patients

Journal of Pediatric and Adolescent Gynecology

Volumn 22, Issue 4, 2009, Pages 229-231

  Nijland, Roel ^a   Hartog, Francis E ^a   Wevers, Ron A ^a   Wanders, Ronald J A ^b   Willemsen, Wim N P ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b EMMA CHILDREN S HOSPITAL   (Netherlands)

Author keywords

Galactose 1 phosphate uridyl transferase; MRKH; M llerian aplasia

Indexed keywords

GALACTITOL; GALACTOSE; GALACTOSE 1 PHOSPHATE URIDYLYLTRANSFERASE; HEMOGLOBIN;

ADULT; APLASIA; ARTICLE; BLOOD SAMPLING; CASE CONTROL STUDY; CLINICAL ARTICLE; CONTROLLED STUDY; DAUGHTER; DIAGNOSTIC VALUE; ENZYME ACTIVITY; FEMALE; HEMOGLOBIN BLOOD LEVEL; HUMAN; KIDNEY AGENESIS; LAPAROSCOPY; LAPAROTOMY; MULLERIAN APLASIA; NETHERLANDS; OUTPATIENT DEPARTMENT; PRIORITY JOURNAL; QUESTIONNAIRE; ROKITANSKY SYNDROME; UNIVERSITY HOSPITAL; URINALYSIS; URINE; VENOUS BLOOD;

ADULT; CASE-CONTROL STUDIES; FEMALE; GALACTOSE; HUMANS; MIDDLE AGED; MULLERIAN DUCTS; NETHERLANDS; POLYMORPHISM, SINGLE NUCLEOTIDE; PREGNANCY; SYNDROME; UTP-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; YOUNG ADULT;

EID: 67651087284     PISSN: 10833188     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpag.2008.10.004     Document Type: Article

References (9)

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