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Results: 1-5 |
Results: 5

Authors: WORTHINGTON S BOWER C HARROP K LOH J WALPOLE I
Citation: S. Worthington et al., 22Q11 DELETIONS IN PATIENTS WITH CONOTRUNCAL HEART-DEFECTS, Journal of paediatrics and child health, 34(5), 1998, pp. 438-443

Authors: COLLEY SMJ WALPOLE I FABIAN VA KAKULAS BA
Citation: Smj. Colley et al., TOPICAL TRETINOIN AND FETAL MALFORMATIONS, Medical journal of Australia, 168(9), 1998, pp. 467-467

Authors: SINGER SL WALPOLE I BROGAN WF GOLDBLATT J
Citation: Sl. Singer et al., DENTOFACIAL FEATURES OF A FAMILY WITH CROUZON SYNDROME - CASE-REPORTS, Australian dental journal, 42(1), 1997, pp. 11-17

Authors: MACRAE FA GARDNER RJM KOOL D WALPOLE I EDKINS E NASIOULAS S
Citation: Fa. Macrae et al., AN EXTREME 3' APC TRUNCATING MUTATION ASSOCIATED WITH AN ATTENUATED FAMILIAL ADENOMATOUS POLYPOSIS (FAP) PHENOTYPE, Gastroenterology, 112(4), 1997, pp. 608-608

Authors: MARTIN RL WALPOLE I GOLDBLATT J
Citation: Rl. Martin et al., IDENTIFICATION OF 2 SPORADICALLY DERIVED MUTATIONS IN THE VON HIPPEL-LINDAU GENE, Human mutation, 7(2), 1996, pp. 185-185
Risultati: 1-5 |