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This Month in Genetics

Garber, Kathryn B.

American journal of human genetics. Volume 92:Issue 6 (2013); pp 837-838 -- Cell Press, Elsevier Inc

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This Month in Genetics

Garber, Kathryn B.

American journal of human genetics. Volume 98:Issue 6 (2016); pp 1049-1050 -- Cell Press, Elsevier Inc

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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies

American journal of human genetics. Volume 99:Issue 2 (2016); pp 287-298 -- Cell Press, Elsevier Inc

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Genes for Good: Engaging the Public in Genetics Research via Social Media

Brieger, Katharine et al.

American journal of human genetics. Volume 105:Number 2 (2019, August 1st); pp 441-442 -- Cell Press, Elsevier Inc

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PIK3R1 Mutations Cause Syndromic Insulin Resistance with Lipoatrophy

Thauvin-Robinet, Christel et al.

American journal of human genetics. Volume 93:Issue 1 (2013); pp 141-149 -- Cell Press, Elsevier Inc

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Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly

Breuss, Martin W. et al.

American journal of human genetics. Volume 99:Issue 1 (2016); pp 228-235 -- Cell Press, Elsevier Inc

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Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome

Zhu, Fuxi et al.

American journal of human genetics. Volume 99:Issue 6 (2016); pp 1405- -- Cell Press, Elsevier Inc

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Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders

Stessman, Holly A.F. et al.

American journal of human genetics. Volume 98:Issue 3 (2016); pp 541-552 -- Cell Press, Elsevier Inc

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Robust Inference of Identity by Descent from Exome-Sequencing Data

Fu, Wenqing et al.

American journal of human genetics. Volume 99:Issue 5 (2016); pp 1106-1116 -- Cell Press, Elsevier Inc

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This Month in Genetics

Garber, Kathryn B.

American journal of human genetics. Volume 100:Issue 1 (2017); pp 3-4 -- Cell Press, Elsevier Inc

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