Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2
© 2020 Elsevier Ltd Objective: Juberg-Hayward syndrome (JHS; MIM 216100) is a rare autosomal recessive malformation syndrome, characterized by cleft lip/palate, microcephaly, ptosis, hypoplasia or aplasia of thumbs, short stature, dislocation of radial head, and fusion of humerus and radius leading...
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Main Authors: | Piranit Nik Kantaputra, Prapai Dejkhamron, Sissades Tongsima, Chumpol Ngamphiw, Worrachet Intachai, Lukana Ngiwsara, Phannee Sawangareetrakul, Jisnuson Svasti, Bjorn Olsen, James R.Ketudat Cairns, Kanokkan Bumroongkit |
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Format: | Journal |
Published: |
2020
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Subjects: | |
Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85091234313&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/70159 |
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Institution: | Chiang Mai University |
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