Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome von Morava, ??va, Czak??, Marta, K??rteszi, Judit, Cser, Beatrix, Weissbecker, Karen, M??hes, Karoly

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Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias) von B hler, Erica M., Luchsinger, Uwe, B hler, Ulrich K., M hes, Karoly, Stalder, Gerhard R.

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Inherited ring chromosomes : an analysis of published cases von KOSZTOLANYI, G, MEHES, K, HOOKE. B

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Premature centromere division of a translocation-carrier autosome von MEHES, K, KOSZTOLANYI, G

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Mild errors of morphogenesis in malignancy: Macroscopic manifestation of genetic instability? von M hes, K roly

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Isolated hypospadias is not associated with signs of midline closure defects von MEHES, K

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Unusually early dividing chromosomes 13?15 in a child with retinoblastoma and 13q delection von M hes, K roly, Bajn czky, Katalin

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Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population von Gyürüs, Péter, Molnár, János, Melegh, Béla, Tóth, Gábor, Morava, Éva, Kosztolányi, György, Méhes, Károly

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Cat-eye syndrome, a partial trisomy 22 von B hler, Erica M., M hes, K roly, M ller, Hansjakob, Stalder, Gerhard R.

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Urinary hydroxyproline and glycosaminoglycan excretion in Down's syndrome von Klujber, L szl, M hes, K roly

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