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1 Ergebnisse
1
Nephrocalcinosis (enamel renal syndrome) caused by autosoma..:
Jaureguiberry, G
;
De la Dure-Molla, M
;
Parry, D
...
info:eu-repo/semantics/altIdentifier/doi/10.1159/000349989. , 2012
Link:
https://serval.unil.ch/notice/serval:BIB_DCEC597C1254
RT Journal T1
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations
UL https://suche.suub.uni-bremen.de/peid=base-ftunivlausanne:oai:serval.unil.ch:BIB_DCEC597C1254&Exemplar=1&LAN=DE A1 Jaureguiberry, G A1 De la Dure-Molla, M A1 Parry, D A1 Quentric, M A1 Himmerkus, N A1 Koike, T A1 Poulter, J A1 Klootwijk, E A1 Robinette, S.L A1 Howie, A.J A1 Patel, V A1 Figueres, M.L A1 Stanescu, H.C A1 Issler, N A1 Nicholson, J.K A1 Bockenhauer, D A1 Laing, C A1 Walsh, S.B A1 McCredie, D.A A1 Povey, S A1 Asselin, A A1 Picard, A A1 Coulomb, A A1 Medlar, A.J A1 Bailleul-Forestier, I A1 Verloes, A A1 Le Caignec, C A1 Roussey, G A1 Guiol, J A1 Isidor, B A1 Logan, C A1 Shore, R A1 Johnson, C A1 Inglehearn, C A1 Al-Bahlani, S A1 Schmittbuhl, M A1 Clauss, F A1 Huckert, M A1 Laugel, V A1 Ginglinger, E A1 Pajarola, S A1 Spartà, G A1 Bartholdi, D A1 Rauch, A A1 Addor, M.C A1 Yamaguti, P.M A1 Safatle, H.P A1 Acevedo, A.C A1 Martelli-Júnior, H A1 dos Santos Netos, P.E A1 Coletta, R.D A1 Gruessel, S A1 Sandmann, C A1 Ruehmann, D A1 Langman, C.B A1 Scheinman, S.J A1 Ozdemir-Ozenen, D A1 Hart, T.C A1 Hart, P.S A1 Neugebauer, U A1 Schlatter, E A1 Houillier, P A1 Gahl, W.A A1 Vikkula, M A1 Bloch-Zupan, A A1 Bleich, M A1 Kitagawa, H A1 Unwin, R.J A1 Mighell, A A1 Berdal, A A1 Kleta, R YR 2012 K1 Adolescent K1 Adult K1 Amelogenesis Imperfecta/complications K1 Amelogenesis Imperfecta/genetics K1 Child K1 Consanguinity K1 Dental Enamel Proteins/genetics K1 Exome/genetics K1 Family Health K1 Female K1 Genes K1 Recessive/genetics K1 Genetic Predisposition to Disease/genetics K1 Genome-Wide Association Study K1 Humans K1 Male K1 Middle Aged K1 Mutation K1 Nephrocalcinosis/complications K1 Nephrocalcinosis/genetics K1 Pedigree K1 Sequence Analysis K1 DNA/methods K1 Syndrome K1 Young Adult JF info:eu-repo/semantics/altIdentifier/doi/10.1159/000349989 LK http://dx.doi.org/https://serval.unil.ch/notice/serval:BIB_DCEC597C1254 DO https://serval.unil.ch/notice/serval:BIB_DCEC597C1254 SF ELIB - SuUB Bremen
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