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Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome Sequencing.
Pediatr Cardiol. 2020 Jan;41(1):165-174. doi: 10.1007/s00246-019-02240-x. Epub 2019 Nov 11.
Pediatr Cardiol. 2020.
PMID: 31712860
A novel DLL4 mutation in Adams-Oliver syndrome with absence of the right pulmonary artery in newborn.
Rojnueangnit K, Phawan T, Khetkham T, Techasatid W, Sirichongkolthong B.
Rojnueangnit K, et al. Among authors: khetkham t.
Am J Med Genet A. 2022 Feb;188(2):658-664. doi: 10.1002/ajmg.a.62562. Epub 2021 Nov 10.
Am J Med Genet A. 2022.
PMID: 34755929
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Genetic diagnosis for adult patients at a genetic clinic.
Rojnueangnit K, Anthanont P, Khetkham T, Puttamanee S, Ittiwut C.
Rojnueangnit K, et al. Among authors: khetkham t.
Cold Spring Harb Mol Case Stud. 2022 Dec 28;8(7):a006235. doi: 10.1101/mcs.a006235. Print 2022 Dec.
Cold Spring Harb Mol Case Stud. 2022.
PMID: 36265913
Free PMC article.
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Two Novel GATA1 Mutations in Transient Abnormal Myelopoiesis of Thai Neonates with Down Syndrome.
Chukua K, Netsawang C, Padungthai K, Khetkham T, Chokevittaya P, Poonjearansilp O, Prachuktum S, Kositamongkol S, Techasatit W, Silapamongkolkul P, Satayasai W, Pusongchai T, Surapolchai P, Rojnueangnit K.
Chukua K, et al. Among authors: khetkham t.
J Pediatr Genet. 2019 Dec;8(4):187-192. doi: 10.1055/s-0039-1696971. Epub 2019 Sep 11.
J Pediatr Genet. 2019.
PMID: 31687255
Free PMC article.
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Clinical Features to Predict 22q11.2 Deletion Syndrome Proven by Molecular Genetic Testing.
Rojnueangit K, Khetkham T, Onsod P, Chareonsirisuthigul T.
Rojnueangit K, et al. Among authors: khetkham t.
J Pediatr Genet. 2020 Oct 1;11(1):22-27. doi: 10.1055/s-0040-1718386. eCollection 2022 Mar.
J Pediatr Genet. 2020.
PMID: 35186386
Free PMC article.
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The First Report of Multicentric Carpotarsal Osteolysis Syndrome Caused by MAFB Mutation in Asian.
Choochuen P, Rojneuangnit K, Khetkham T, Khositseth S.
Choochuen P, et al. Among authors: khetkham t.
Case Rep Med. 2018 Sep 16;2018:6783957. doi: 10.1155/2018/6783957. eCollection 2018.
Case Rep Med. 2018.
PMID: 30305815
Free PMC article.
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