To see an article, click its [Full Text] or [PDF] link. To review many abstracts, check the boxes to the left of the titles you want, and click the 'Get All Checked Abstract(s)' button. To see one abstract at a time, click its [Abstract] link.

Review articles

	Genetic susceptibility to age related macular degeneration John R W Yates and Anthony T Moore J Med Genet 2000; 37: 83-87. doi:10.1136/jmg.37.2.83 [Abstract] [Full text] [PDF] [Request Permissions]

Commentaries

	Of palms, soles, and gums ROBERT J GORLIN J Med Genet 2000; 37: 81-82. doi:10.1136/jmg.37.2.81 [Extract] [Full text] [PDF] [Request Permissions]

Original articles

	Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C T C Hart, P S Hart, M D Michalec, Y Zhang, E Firatli, T E Van Dyke, A Stabholz, A Zlorogorski, L Shapira, and W A Soskolne J Med Genet 2000; 37: 88-94. doi:10.1136/jmg.37.2.88 [Abstract] [Full text] [PDF] [Request Permissions]
	Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation T C Hart, P S Hart, M D Michalec, Y Zhang, M L Marazita, M Cooper, O M Yassin, M Nusier, and S Walker J Med Genet 2000; 37: 95-101. doi:10.1136/jmg.37.2.95 [Abstract] [Full text] [PDF] [Request Permissions]
	Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by  sarcoglycan mutations Rita Barresi, Claudia Di Blasi, Tiziana Negri, Raffaella Brugnoni, Andrea Vitali, Giorgio Felisari, Antonio Salandi, Sergio Daniel, Ferdinando Cornelio, Lucia Morandi, and Marina Mora J Med Genet 2000; 37: 102-107. doi:10.1136/jmg.37.2.102 [Abstract] [Full text] [PDF] [Request Permissions]
	Evaluation of a counselling protocol for predictive genetic testing for hereditary non-polyposis colorectal cancer Katja Aktan-Collan, Jukka-Pekka Mecklin, Albert de la Chapelle, Päivi Peltomäki, Antti Uutela, and Helena Kääriäinen J Med Genet 2000; 37: 108-113. doi:10.1136/jmg.37.2.108 [Abstract] [Full text] [PDF] [Request Permissions]
	Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH Pawel Stankiewicz, Ewa Bocian, Krystyna Jakubów-Durska, Ewa Obersztyn, Ewa Lato, Heike Starke, Katarzyna Mroczek, and Tadeusz Mazurczak J Med Genet 2000; 37: 114-120. doi:10.1136/jmg.37.2.114 [Abstract] [Full text] [PDF] [Request Permissions]
	A supernumerary marker chromosome originating from two different regions of chromosome 18 Benno Röthlisberger, Krystyna Chrzanowska, Damina Balmer, Mariluce Riegel, and Albert Schinzel J Med Genet 2000; 37: 121-124. doi:10.1136/jmg.37.2.121 [Abstract] [Full text] [PDF] [Request Permissions]

Short reports

	5p14 deletion associated with microcephaly and seizures Elizabeth I Johnson, R Catrinel Marinescu, Hope H Punnett, Beverly Tenenholz, and Joan Overhauser J Med Genet 2000; 37: 125-127. doi:10.1136/jmg.37.2.125 [Abstract] [Full text] [PDF] [Request Permissions]
	A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome Dmitry Tentler, Peter Gustavsson, Göran Elinder, Ole Eklöf, Laurie Gordon, Ariane Mandel, and Niklas Dahl J Med Genet 2000; 37: 128-131. doi:10.1136/jmg.37.2.128 [Abstract] [Full text] [PDF] [Request Permissions]
	First description of germline mosaicism in familial hypertrophic cardiomyopathy Jean-François Forissier, Pascale Richard, Sylvain Briault, Céline Ledeuil, Olivier Dubourg, Bernard Charbonnier, Lucie Carrier, Claude Moraine, Gisèle Bonne, Michel Komajda, Ketty Schwartz, and Bernard Hainque J Med Genet 2000; 37: 132-134. doi:10.1136/jmg.37.2.132 [Abstract] [Full text] [PDF] [Request Permissions]

Perspectives

	Shared decision making and non-directiveness in genetic counselling Glyn Elwyn, Jonathon Gray, and Angus Clarke J Med Genet 2000; 37: 135-138. doi:10.1136/jmg.37.2.135 [Extract] [Full text] [PDF] [Request Permissions]

Letters to the editor

	The CAG repeat within the androgen receptor gene in male breast cancer patients I E YOUNG, K M KURIAN, M A F MACKENZIE, I H KUNKLER, B B COHEN, M L HOOPER, A H WYLLIE, and C M STEEL J Med Genet 2000; 37: 139-140. doi:10.1136/jmg.37.2.139 [Extract] [Full text] [PDF] [Request Permissions]
	Deletion and duplication of the adenomatous polyposis coli gene resulting from an interchromosomal insertion involving 5(q22q23.3) in the father R J HASTINGS, E C SVENNEVIK, B SETTERFIELD, D WELLS, J D A DELHANTY, and H MACKINNON J Med Genet 2000; 37: 141-145. doi:10.1136/jmg.37.2.141 [Extract] [Full text] [PDF] [Request Permissions]
	Hypoparathyroidism, retarded growth and development, and dysmorphism or Sanjad-Sakati syndrome: an Arab disease reminiscent of Kenny-Caffey syndrome AHMAD S TEEBI J Med Genet 2000; 37: 145. doi:10.1136/jmg.37.2.145 [Extract] [Full text] [PDF] [Request Permissions]
	Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B) MICHEL BAHUAU, INGRID LAURENDEAU, ANNA PELET, BRIGITTE ASSOULINE, THIERRY LAMIREAU, LAURENCE TAINE, BRIGITTE LE BAIL, PIERRE VERGNES, SERGE GALLET, MICHEL VIDAUD, STANISLAS LYONNET, DIDIER LACOMBE, and DOMINIQUE VIDAUD J Med Genet 2000; 37: 146-150. doi:10.1136/jmg.37.2.146 [Extract] [Full text] [PDF] [Request Permissions]
	Identification of novel alleles at a polymorphic microsatellite repeat region in the human NRAMP1 gene promoter: analysis of allele frequencies in primary biliary cirrhosis A M GRAHAM, M M DOLLINGER, S E M HOWIE, and D J HARRISON J Med Genet 2000; 37: 150-152. doi:10.1136/jmg.37.2.150 [Extract] [Full text] [PDF] [Request Permissions]
	No evidence for imprinting in distal 18q ROBERT MAIWALD, JOAN OVERHAUSER, and FRANCO LACCONE J Med Genet 2000; 37: 152-156. doi:10.1136/jmg.37.2.152 [Extract] [Full text] [PDF] [Request Permissions]
	Renal angiomyolipomata and learning difficulty in tuberous sclerosis complex FINBAR J K O'CALLAGHAN, MICHAEL NOAKES, and JOHN P OSBORNE J Med Genet 2000; 37: 156-157. doi:10.1136/jmg.37.2.156 [Extract] [Full text] [PDF] [Request Permissions]
	Clinical geneticists' attitudes and practice towards testing for breast cancer susceptibility genes ANNEKE M LUCASSEN and RICHARD S HOULSTON J Med Genet 2000; 37: 157-160. doi:10.1136/jmg.37.2.157 [Extract] [Full text] [PDF] [Request Permissions]

To see an article, click its [Full Text] or [PDF] link. To review many abstracts, check the boxes to the left of the titles you want, and click the 'Get All Checked Abstract(s)' button. To see one abstract at a time, click its [Abstract] link.