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2002
Mark ABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosis
Visapaa, Ilona ; Fellman, Vineta ^LU ; Lanyi, Lisa and Peltonen, Leena (2002) In American Journal of Medical Genetics 109(3). p.202-205
- Contribution to journal › Article
Mark Analysis of ten candidate genes in autism by association and linkage
Philippe, Anne ; Guilloud-Bataille, Michel ; Martinez, Maria ; Gillberg, Christopher ; Råstam, Maria ^LU ; Sponheim, Eili ; Coleman, Mary ; Zappella, Michele ; Aschauer, Harald and Penet, Christiane , et al. (2002) In American Journal of Medical Genetics 114(2). p.125-128
- Contribution to journal › Article
2001
Mark VATER non-random association of congenital malformations: study based on data from four malformation registers
Källén, Karin ^LU ; Mastroiacovo, Pierpaolo ; Castilla, Eduardo E. ; Robert, Elisabeth and Källén, Bengt ^LU (2001) In American Journal of Medical Genetics 101(1). p.26-32
- Contribution to journal › Article
Mark Isolated glycerol kinase deficiency and fanconi anemia [1]
Sjarif, D. R. ; Révész, T. ; de Koning, T. J. ^LU ; Duran, M. ; Beemer, F. A. and Poll-The, B. T. (2001) In American Journal of Medical Genetics 99(2). p.159-160
- Contribution to journal › Letter
2000
Mark OEIS complex--a population study
Källén, Karin ^LU ; Castilla, E E ; Robert, E ; Mastroiacovo, P and Kallen, B (2000) In American Journal of Medical Genetics 92(1). p.62-68
- Contribution to journal › Article
1995
Mark Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis
De Koning, T. J. ^LU ; Sandkuijl, L. A. ; De Schryver, J. E.A.R. ; Hennekam, E. A.M. ; Beemer, F. A. and Houwen, R. H.J. (1995) In American Journal of Medical Genetics 57(3). p.479-482
- Contribution to journal › Article