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Human Heredity|April 27, 2000
Identification of a prevalent nonsense mutation (W283X) and two novel mutations in the porphobilinogen deaminase gene of Swiss patients with acute intermittent porphyriaX Schneider-Yin, C Bogard, U B Rüfenacht, et al.Human Heredity|May 19, 2001
Mutation analysis of a Mauritian hereditary breast cancer family reveals the BRCA2 6503deITT mutation previously found to recur in different ethnic populationsG Khittoo, A Manning, H Mustun, et al.Human Heredity|October 6, 2001
Case-control studies of genetic markers: power and sample size approximations for Armitage's test for trendS L Slager, D J SchaidHuman Heredity|January 24, 2021
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan FamilySoukaina Elrharchi, Zied Riahi, Sara Salime, et al.Human Heredity|January 1, 1988
Relationship between placental alkaline phosphatase types and obstetric history of motherP P BalgirHuman Heredity|January 1, 1988
Complement C4 phenotypes in dementia of the Alzheimer typeP Eikelenboom, J Goetz, J C Pronk, et al.Human Heredity|January 1, 1988
Transferrin C2 and radiation-induced chromosomal damageL Beckman, I NordensonHuman Heredity|August 30, 2019
A Low-Rank Representation Method Regularized by Dual-Hypergraph Laplacian for Selecting Differentially Expressed GenesXiu-Xiu Xu, Ling-Yun Dai, Xiang-Zhen Kong, et al.Human Heredity|January 1, 1978
Group-specific component, alpha1-antitrypsin and esterase D in Canadian EskimosD W Cox, N E Simpson, R JanttiHuman Heredity|January 1, 1978
Alpha-1-antitrypsin phenotypes in newborns from Central and Southern ItalyM Piantelli, P Auconi, P MusianiPageof 237