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Results:
1-7
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Results: 7
Authors:
NJOLSTAD PR
COCKBURN BN
BELL GI
SOVIK O
Citation: Pr. Njolstad et al., A MISSENSE MUTATION, VAL62ALA, IN THE GLUCOKINASE GENE IN A NORWEGIANFAMILY WITH MATURITY-ONSET DIABETES OF THE YOUNG, Acta paediatrica, 87(8), 1998, pp. 853-856
Authors:
NJOLSTAD PR
REIGSTAD H
WESTBY J
ESPELAND A
Citation: Pr. Njolstad et al., FAMILIAL NONIMMUNE HYDROPS-FETALIS AND CONGENITAL PULMONARY LYMPHANGIECTASIA, European journal of pediatrics, 157(6), 1998, pp. 498-501
Authors:
JOHNSON D
HORSLEY SW
MOLONEY DM
OLDRIDGE M
TWIGG SRF
WALSH S
BARROW M
NJOLSTAD PR
KUNZ J
ASHWORTH GJ
WALL SA
KEARNEY L
WILKIE AOM
Citation: D. Johnson et al., A COMPREHENSIVE SCREEN FOR TWIST MUTATIONS IN PATIENTS WITH CRANIOSYNOSTOSIS IDENTIFIES A NEW MICRODELETION SYNDROME OF CHROMOSOME BAND 7P21.1, American journal of human genetics, 63(5), 1998, pp. 1282-1293
Authors:
NJOLSTAD PR
SKJELDAL OH
AGSTERIBBE E
HUCKRIEDE A
WANNAG E
SOVIK O
WAALER PE
Citation: Pr. Njolstad et al., MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY AND FATAL VALPROATE TOXICITY, Pediatric neurology, 16(2), 1997, pp. 160-162
Authors:
NJOLSTAD PR
SKJELDAL OH
AGSTERIBBE E
HUCKRIEDE A
WANNAG E
SOVIK O
WAALER PE
Citation: Pr. Njolstad et al., MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY AND FATAL VALPROATE TOXICITY, Pediatric neurology, 16(2), 1997, pp. 160-162
Authors:
HASSOUN H
VASSILIADIS JN
MURRAY J
NJOLSTAD PR
ROGUS JJ
BALLAS SK
SCHAFFER F
JAROLIM P
BRABEC V
PALEK J
Citation: H. Hassoun et al., CHARACTERIZATION OF THE UNDERLYING MOLECULAR DEFECT IN HEREDITARY SPHEROCYTOSIS ASSOCIATED WITH SPECTRIN DEFICIENCY, Blood, 90(1), 1997, pp. 398-406
Authors:
MOLVEN A
HORDVIK I
NJOLSTAD PR
Citation: A. Molven et al., SEQUENCE-ANALYSIS OF THE ZEBRAFISH HOX-B5 B6 REGION/, Biochimica et biophysica acta, 1173(1), 1993, pp. 102-106
Risultati:
1-7
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