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Issues
March 1999
ISSN 0001-5652
EISSN 1423-0062
In this Issue
Journal Name Change
Vol. 1-18 (1948/1950-1968) were published under the journal's former title Acta Genetica et Statistica Medica.
Human Heredity 1999, Vol. 49, No. 2
Original Paper
True Pedigree Errors More Frequent Than Apparent Errors for Single Nucleotide Polymorphisms
Subject Area:
Genetics
Hum Hered (1999) 49 (2): 65–70.
https://doi.org/10.1159/000022846
Molecular Genetic Study of Autosomal Dominant Retinitis pigmentosa in Lithuanian Patients
Subject Area:
Genetics
Vaidutis Kučinskas; AnnetteM. Payne; Daiva Ambrasienė; Vaclovas Jurgelevičius; Danguolė Steponavičiūtė; JulijaVidutė Arčiulienė; Emilija Daktaravičienė; Shomi Bhattacharya
Hum Hered (1999) 49 (2): 71–74.
https://doi.org/10.1159/000022847
Human NDUFB9 Gene: Genomic Organization and a Possible Candidate Gene Associated with Deafness Disorder Mapped to Chromosome 8q13
Subject Area:
Genetics
Hum Hered (1999) 49 (2): 75–80.
https://doi.org/10.1159/000022848
Analysis of the Complete Coding Region of the CFTR Gene in Ten Algerian Cystic Fibrosis Families
Subject Area:
Genetics
Hum Hered (1999) 49 (2): 81–84.
https://doi.org/10.1159/000022849
Contribution of Interleukin 1β and KM Loci to Alopecia areata
Subject Area:
Genetics
Hum Hered (1999) 49 (2): 85–89.
https://doi.org/10.1159/000022850
Linkage Disequilibrium and Haplotype Analysis in German Friedreich Ataxia Families
Subject Area:
Genetics
Christine Zühlke; Ulrike Gehlken; Sabine Purmann; Markus Kunisch; Bertram Müller-Myhsok; Friedmar Kreuz; Franco Laccone
Hum Hered (1999) 49 (2): 90–96.
https://doi.org/10.1159/000022851
Hereditary Desmoid Disease in a Family with a Germline Alu I Repeat Mutation of the APC Gene
Subject Area:
Genetics
Kevin C. Halling; Carlo R. Lazzaro; Ronald Honchel; José A. Bufill; Steven M. Powell; Carola A.S. Arndt; Noralane M. Lindor
Hum Hered (1999) 49 (2): 97–102.
https://doi.org/10.1159/000022852
No Correlation between A(–1438)G Polymorphism in 5-HT2A Receptor Gene Promoter and the Density of Frontal Cortical 5-HT2A Receptors in Schizophrenia
Subject Area:
Genetics
Alexander P. Kouzmenko; Antonietta Scaffidi; AvrilM. Pereira; Wendy L. Hayes; David L. Copolov; Brian Dean
Hum Hered (1999) 49 (2): 103–105.
https://doi.org/10.1159/000022853
A Principal-Components Approach Based on Heritability for Combining Phenotype Information
Subject Area:
Genetics
Hum Hered (1999) 49 (2): 106–111.
https://doi.org/10.1159/000022854
Linkage Information Content of Polymorphic Genetic Markers
Subject Area:
Genetics
Hum Hered (1999) 49 (2): 112–118.
https://doi.org/10.1159/000022855
Mutation Report
A Novel Splice Site Mutation in a Brazilian Patient with Hereditary Antithrombin Deficiency Type I
Subject Area:
Genetics
Hum Hered (1999) 49 (2): 119–120.
https://doi.org/10.1159/000022856
A Novel Nonsense Mutation 6, E – X in the Protein S Gene Causes Type I Deficiency
Subject Area:
Genetics
Hum Hered (1999) 49 (2): 121–122.
https://doi.org/10.1159/000022857
