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Publisher: Blackwell Publishing

Volume 55, Number 4, April 1999
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Biology of presenilins as causative molecules for Alzheimer disease
pp. 219-225(7)
Authors: Nishimura, Masaki; Yu, Gang; St George-Hyslop, Peter H

HotSpots
pp. 226-230(5)
Author: Leavitt, Blair

Genetic landmarks through philately - a brief history of diabetes mellitus
pp. 231-233(3)
Author: Chudley, Albert E

The assent of a nation: genethics and Iceland
pp. 234-239(6)
Author: McInnis, Melvin G

Autosomal dominant cataracts and Peters anomaly in a large Australian family
pp. 240-247(8)
Authors: Withers, Stephen J; Gole, Glen A; Summers, Kim M

Linkage disequilibrium mapping of the Nova Scotia variant of Niemann-Pick disease
pp. 248-255(8)
Authors: Greer, WL; Riddell, DC; Murty, S; Gillan, TL; Girouard, GS; Sparrow, SM; Tatlidil, C; Dobson, MJ; Neumann, PE

A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysis
pp. 256-258(3)
Authors: Paoloni-Giacobino, A; Dutoit, Mh; Morris, Ma; Dahoun, Sp

Procedure to protect confidentiality of familial data in community genetics and genomic research
pp. 259-264(6)
Authors: Gaudet, Daniel; Arsenault, Steve; Bélanger, Céline; Hudson, Thomas; Perron, Patrice; Bernard, Manon; Hamet, Pavel

An unbalanced half-cryptic translocation involving the 6q subtelomeric region and 2p25.3 in a child with mental retardation: uses and limitations of fluorescence insitu hybridization
pp. 265-268(4)
Authors: Batanian, JR; Hussain, MI

Partial DiGeorge syndrome in two patients with a 10p rearrangement
pp. 269-276(8)
Authors: Van Esch, Hilde; Groenen, Peter; Daw, Sarah; Poffyn, Ann; Holvoet, Maureen; Scambler, Peter; Fryns, Jean-Pierre; Van de Ven, Wim; Devriendt, Koen

Clinical characteristics of Angelman syndrome patients with a non-IC-deleted imprinting mutation
pp. 277-278(2)

Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity
pp. 279-280(2)

FokI polymorphism at the human vitamin D receptor gene locus in Europeans and Africans
pp. 281-282(2)

Tetrasomy 21pter-q22.11: molecular, cytogenetic, and clinical findings
pp. 283-286(4)

British Human Genetics Conference
pp. 287-287(1)

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Key:
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