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Molekylärgenetik vid långt QT-syndrom. Gener som orsakar svimning och plötsligt död
Molecular genetics of the long QT syndrome. Genes causing syncope and sudden death

Fosdal, I ; Wetrell, G ; Christiansen, M ; Kanters, J K ; Larsen, L A

Läkartidningen, 2001, Vol.98(8) [Peer Reviewed Journal]

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Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

Larsen, L A ; Fosdal, I ; Andersen, P S ; Kanters, J K ; Vuust, J ; Wettrell, G ; Christiansen, M Larsen, L A (correspondence author) ; Larsen, L A (record owner)

European journal of human genetics : EJHG, September 1999, Vol.7(6), pp.724-728 [Peer Reviewed Journal]

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Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity.

Grigelioniene, G ; Schoumans, J ; Neumeyer, L ; Ivarsson, A ; Eklöf, O ; Enkvist, O ; Tordai, P ; Fosdal, I ; Myhre, A G ; Westphal, O ; Nilsson, N O ; Elfving, M ; Ellis, I ; Anderlid, B M ; Fransson, I ; Tapia-Paez, I ; Nordenskjöld, M ; Hagenäs, L ; Dumanski, J P Grigelioniene, G (correspondence author) ; Grigelioniene, G (record owner)

Human genetics, November 2001, Vol.109(5), pp.551-558 [Peer Reviewed Journal]

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