Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fcγ receptor gene region Roger V. LeboPhillip F. ChanceP. Michael Conneally Original Investigations Pages: 1 - 12
Multicolor fluorescence in situ hybridization and pulsed field electrophoresis dissect CMT1B gene region Roger V. LeboEric D. LynchMels van der Ploeg Original Investigations Pages: 13 - 20
Relative order determination of four Yp cosmids on metaphase and interphase chromosomes by two-color competitive in situ hybridization R. SlimJ. WeissenbachA. Bernheim Original Investigations Pages: 21 - 26
Chromosome arrangements in human fibroblasts at mitosis W. MosgöllerA. R. LeitchJ. S. Heslop-Harrison Original Investigations Pages: 27 - 33
Genotypic analysis of families with lactate dehydrogenase A(M) deficiency by selective DNA amplification Masato MaekawaKayoko SudoTakashi Kanno Original Investigations Pages: 34 - 38
Chromosomal instability in breast cancer patients Leonardo BarriosM. R. CaballínJosep Egozcue Original Investigations Pages: 39 - 41
Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome C. A. GregoryJ. SchwartzJ. L. Hamerton Original Investigations Pages: 42 - 48
Chromosomal mosaicism: a follow-up study of 39 unselected children found at birth Claus H. GravholtUrsula FriedrichJohannes Nielsen Original Investigations Pages: 49 - 52
Human dystrophin gene transfer: production and expression of a functional recombinant DNA-based gene George DicksonDonald R. LoveFrank S. Walsh Original Investigations Pages: 53 - 58
Comparative mapping of ZFY in the hominoid apes Gaby MüllerWerner Schempp Original Investigations Pages: 59 - 63
A test of the production line hypothesis of mammalian oogenesis Paul E. PolaniJohn A. Crolla Original Investigations Pages: 64 - 70
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17 Manuela C. KochKenneth RickerEric P. Hoffman Original Investigations Pages: 71 - 74
Hypercholesterolemia in five Israeli Christian-Arab kindreds is caused by the “Lebanese” allele at the low density lipoprotein receptor gene locus and by an additional independent major factor Arie OppenheimYechiel FriedlanderEran Leitersdorf Original Investigations Pages: 75 - 84
A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locus R. FahsoldH. -D. RottP. Lorenz Original Investigations Pages: 85 - 90
Phenylketonuria in Poland: 66% of PKU alleles are caused by three mutations Marta ZygulskaAntonin EigelJürgen Horst Original Investigations Pages: 91 - 94
Confirmation of the chromosomal localization of human lamp genes and their exclusion as candidate genes for Salla disease Johanna SchleutkerLeena HaatajaPertti Aula Original Investigations Pages: 95 - 97
Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy B. A. KormannH. SchusterB. Leo-Kottler Original Investigations Pages: 98 - 100
The human cardiac troponin I locus: assignment to chromosome 19p13.2–19q13.2 Catriona MacGeochPaul J. R. BartonNigel K. Spurr Original Investigations Pages: 101 - 104
Differential methylation at the 5′ and the 3′ CCGG sites flanking the X chromosomal hypervariable DXS255 locus R. W. HendriksM. E. M. KraakmanR. K. B. Schuurman Original Investigations Pages: 105 - 111
Regional mapping of 22 microclones around the adenomatous polyposis coli (APC) locus on chromosome 5q Garret M. HamptonCathy HoweWolfgang G. Ballhausen Short Communications Pages: 112 - 114
Trisomy 16q23→qter arising from a maternal t(13;16)(p12;q23): case report and evidence of the reciprocal balanced maternal rearrangement by the Ag-NOR technique J. B. SavaryF. VasseurM. M. Deminatti Short Communications Pages: 115 - 118
Chromosome mapping of the human cytidine-5′-triphosphate synthetase (CTPS) gene to band 1p34.1–p34.3 by fluorescence in situ hybridization Ei-ichi TakahashiMasatake YamauchiTada-aki Hori Short Communications Pages: 119 - 121
A rare insertional translocation of proximal segment with heterochromatic region of 1q into 7p in monozygotic twins and spontaneous abortions Razia S. MuneerLora M. ThompsonE. Kamat Clinical Case Report Pages: 122 - 123
C-anaphase versus premature centromere division H. RiveraM. G. Dominguez Letter to the Editors Pages: 124 - 124