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American Journal of Human Genetics|May 8, 2021
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunctionBobby G Ng, Paulina Sosicka, François Fenaille, et al.American Journal of Human Genetics|June 24, 2020
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft TriosMadison R Bishop, Kimberly K Diaz Perez, Miranda Sun, et al.American Journal of Human Genetics|November 1, 1981
A study of cardiovascular risk in heterozygotes for homocystinuriaS H Mudd, R Havlik, H L Levy, et al.American Journal of Human Genetics|November 1, 1981
Evidence for heterosis in the HLA systemF L Black, F M SalzanoAmerican Journal of Human Genetics|September 1, 1978
Phenotype dependence in the inhibition of red cell acid phosphatase (ACP) by folatesG F Sensabaugh, V L GoldenAmerican Journal of Human Genetics|January 1, 1980
Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblastsB Wolf, H F Willard, L E RosenbergAmerican Journal of Human Genetics|January 1, 1980
Schizophrenia: the systematic construction of genetic modelsJ StewartAmerican Journal of Human Genetics|January 1, 1980
Properties of fetal and adult red blood cell arginase: a possible prenatal diagnostic test for arginase deficiencyE B Spector, M Kiernan, B Bernard, et al.American Journal of Human Genetics|July 1, 1985
Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuriaA S Lidsky, F D Ledley, A G DiLella, et al.American Journal of Human Genetics|July 1, 1985
A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probesJ Feder, L Yen, E Wijsman, et al.Pageof 979