Regional mapping of the gene for human lysosomal acid phosphatase (ACP2) using a hybrid clone panel containing segments of human chromosome 11 Carol JonesFa-Ten Kao Original Investigations Pages: 1 - 10
Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita Shiro MiwaHisaichi FujiiMitsuyuki Fukuda Original Investigations Pages: 11 - 17
Differential staining in the secondary constriction regions of human chromosomes A1, C9, and E16 by a heat-hypotonic treatment technique N. Kanda Original Investigations Pages: 19 - 24
Deficiency of DNA ligase activity in Fanconi's anemia Monica Hirsch-KauffmannManfred SchweigerKarl Sperling Original Investigations Pages: 25 - 32
A cytogenetic survey of an institution for the mentally retarded Janice MatsuuraMartha MayerPatricia Jacobs Original Investigations Pages: 33 - 41
Inversions and other unusual heteromorphisms detected by C-banding Martha MayerJanice MatsuuraPatricia Jacobs Original Investigations Pages: 43 - 50
The problem of partial endoreduplication Christine Stahl-MaugéH. D. HagerTraute M. Schroeder Original Investigations Pages: 51 - 62
Gene dosage effect for human triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in partial trisomy 12p13 and trisomy 18p Françoise ServilleClaudine JunienA. Broustet Original Investigations Pages: 63 - 69
Brother and sister with trisomy 10p P. de ChieriE. SpatuzzaJ. M. Bonich Original Investigations Pages: 71 - 75
GLO polymorphism in two Polish population samples P. KozioŀT. Dobosz Short Communications Pages: 77 - 79
A new rare phenotype of glycine-rich β-glycoprotein R. ScherzR. PflugshauptR. Bütler Short Communications Pages: 81 - 83
Anencephaly in trisomy 18 associated with elevated alpha-1-fetoprotein in amniotic fluid Ulrik MerrildVibeke SchiølerCarl Johan Edeling Clinical Case Reports Pages: 85 - 88
Partial trisomies 13 and 22 due to nondisjunction of a maternal reciprocal translocation, t(13;22)(q22;q11) Osvaldo MutchinickLizbeth RuzRamón Jiménez Clinical Case Reports Pages: 89 - 95
The problem of partial trisomy 22 reconsidered G. M. FeldmanR. S. Sparkes Clinical Case Reports Pages: 97 - 101
Rapidly adhering cells in two cases of anencephaly Theda VoigtländerUrsula MüllerTraute M. Schroeder Clinical Case Reports Pages: 107 - 110