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Item hits:
Issue Date
Title
Author(s)
1-Jan-2020
Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation --<sup>SEA</sup>/--<sup>CR</sup>, a novel α<sup>0</sup>-thalassemia deletion
Chedtapak Ruengdit
;
Sitthichai Panyasai
;
Naowarat Kunyanone
;
Worawich Phornsiricharoenphant
;
Chumpol Ngamphiw
;
Sissades Tongsima
;
Orapan Sripichai
;
Serge Pissard
;
Sakorn Pornprasert
1-Nov-2020
Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2
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
Discover
Author
2
Chumpol Ngamphiw
1
Bjorn Olsen
1
Chedtapak Ruengdit
1
James R.Ketudat Cairns
1
Jisnuson Svasti
1
Kanokkan Bumroongkit
1
Lukana Ngiwsara
1
Naowarat Kunyanone
1
Orapan Sripichai
1
Phannee Sawangareetrakul
.
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Subject
1
Dentistry