Search  -  prev / next

virtual library in human genetics and molecular biology

International Journal of Human and Medical Genetics

Original Papers

¹⁶⁰Thr Mutation in the Rhodopsin Gene Associated with Retinitis pigmentosa
Capeans, C.; Blanco, M.J.; Lareu, M.V.; Salas, A.; Piñeiro, A.; Sánchez-Salorio, M.; Carracedo, A. (Santiago de Compostela)


Repetitive Exon 45/46-Related Sequences of Human Ca²⁺ Channel a_1C Subunit Gene
Soldatov, N.M. (Washington, D.C.); Raudsepp, T.; Chowdhary, B.P. (Uppsala)


New DNA Polymorphisms Define Ethnically Distinct Haplotypes in the Human Transferrin Receptor Gene
Van Landeghem, G.F.; Beckman, L.E.; Sikström, C. (Umeå); Saha, N. (Singapore); Kucinskas, V. (Vilnius); Beckman, L. (Umeå)


Adult-Onset Primary Open Angle Glaucoma Does Not Localize to Chromosome 2cen-q13 in North American Families
Allingham, R.R. (Durham, N.C.); Wiggs, J.L. (Boston, Mass.); Damji, K.F.; Herndon, L.; Youn, J.; Tallett, D.A.; Jones, K.H. (Durham, N.C.); Del Bono, E.A.; Reardon, M. (Boston, Mass.); Haines, J.L. (Nashville, Tenn.); Pericak-Vance, M.A. (Durham, N.C.)


DNA Analysis of the Fragile X Syndrome in an at Risk Pediatric Population in Croatia: Simple Clinical Preselection Criteria Can Considerably Improve the Cost-Effectiveness of Fragile X Screening Studies
Hecimovic, S.; Barisic, I.; Pavelic, K. (Zagreb)


Low-Order Polynomial Trends of Female-to-Male Map Distance Ratios along Human Chromosomes
Li, W. (New York, N.Y.); Fann, C.S.J. (Bronx, N.Y.); Ott, J. (New York, N.Y.)


No Evidence for an Association between a Variant of the Mast Cell Chymase Gene and Atopic Dermatitis Based on Case-Control and Haplotype-Relative-Risk Analyses
Kawashima, T.; Noguchi, E.; Arinami, T.; Kobayashi, K.; Otsuka, F.; Hamaguchi, H. (Tsukuba)


Multi-Locus Nonparametric Linkage Analysis of Complex Trait Loci with Neural Networks
Lucek, P. (New York, N.Y.); Hanke, J.; Reich, J. (Berlin-Buch); Solla, S.A. (Chicago, Ill./Evanston, Ill.); Ott, J. (New York, N.Y.)



Mutation Report

A Novel in Frame Deletion of Codons 188–190 in the hMSH2 Gene of a Slovenian Patient with Hereditary Non-Polyposis Colorectal Cancer
Ravnik-Glavac, M.; Potocnik, U.; Kozelj, M.; Krizman, I.; Glavac, D. (Ljubljana)

Short Communications

Identification of a CA/TG Repeat Polymorphism Proximal to the Human DLX3 Gene
Price, J.A.; Bowden, D.W.; Hart, T.C. (Winston-Salem, N.C.)

Detection of the apoB-3500 Mutation in a Russian Family with Coronary Heart Disease
Pogoda, T.; Metelskaya, V.; Perova, N.; Limborska, S. (Moscow)

Letter to the Editor

Parental HLA Genes, Hormone Level and Offspring Sex Ratios: A Reply to James’ Letter
Astolfi, P.; Cuccia, M.; Martinetti, M. (Pavia)

Generated by documents 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995-2023 HUM-MOLGEN. All rights reserved. Liability and Copyright.