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American Journal of Human Genetics|January 29, 2002
Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defectsMichael R DeBaun, Emily L Niemitz, D Elizabeth McNeil, et al.
American Journal of Human Genetics|January 1, 1989
On the genetics of prelingual deafnessP P Majumder, A Ramesh, D Chinnappan
American Journal of Human Genetics|November 7, 2017
Inferring Relevant Cell Types for Complex Traits by Using Single-Cell Gene ExpressionDiego Calderon, Anand Bhaskar, David A Knowles, et al.
American Journal of Human Genetics|December 1, 1988
HLA-DR typing "at the DNA level": RFLPs and subtypes detected with a DR beta cDNA probeN J Cox, A P Mela, C M Zmijewski, et al.
American Journal of Human Genetics|February 1, 1989
Two point mutations are responsible for G6PD polymorphism in SardiniaG De Vita, M Alcalay, M Sampietro, et al.
American Journal of Human Genetics|February 1, 1989
The economics of clinical genetics services. III. Cognitive genetics services are not self-supportingB A Bernhardt, R E Pyeritz
American Journal of Human Genetics|November 14, 2017
Functional Consequences of CHRNA7 Copy-Number Alterations in Induced Pluripotent Stem Cells and Neural Progenitor CellsMadelyn A Gillentine, Jiani Yin, Aleksandar Bajic, et al.
American Journal of Human Genetics|May 1, 1988
Haplotypes of the coagulation factor XIII A subunit locus in normal and deficient subjectsP G Board, R Chapple, M Coggan
American Journal of Human Genetics|May 1, 1988
An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequenceM D'Urso, L Luzzatto, L Perroni, et al.
American Journal of Human Genetics|October 3, 2017
Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal DefectsRoberta De Mori, Marta Romani, Stefano D'Arrigo, et al.
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