Theresa Mihalic Mosher
3PUBLICATIONS
17CO-AUTHORS
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Publications (3)
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|Dec 03, 2021
Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactyly.Marilena Melas, Esko A Kautto, Samuel J Franklin
|Jul 07, 2019
Expansion of B4GALT7 linkeropathy phenotype to include perinatal lethal skeletal dysplasia.Theresa Mihalic Mosher, Deborah A Zygmunt, Daniel C Koboldt
|May 06, 2018
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder.Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado
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Frequent Collaborators
3 joint publications
Peter White
2 joint publications
Kim L McBride
1 joint publications
Annick Toutain
1 joint publications
Eric Haan
1 joint publications
Jozef Gecz
1 joint publications
Vera M Kalscheuer
1 joint publications
Marilena Melas
1 joint publications
Esko A Kautto
1 joint publications
Samuel J Franklin
1 joint publications
Mari Mori
