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1 Ergebnisse
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Molecular diagnosis of hereditary spherocytosis by multi-ge..:
Choi, Hyoung Soo
;
Choi, Qute
;
Kim, Jung-Ah
...
Orphanet Journal of Rare Diseases. 14(1):114. , 2019
Link:
http://hdl.handle.net/10371/156024
RT Journal T1
Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte
UL https://suche.suub.uni-bremen.de/peid=base-ftseoulnuniv:oai:s-space.snu.ac.kr:10371_156024&Exemplar=1&LAN=DE A1 Choi, Hyoung Soo A1 Choi, Qute A1 Kim, Jung-Ah A1 Im, Kyong Ok A1 Park, Si Nae A1 Park, Yoomi A1 Shin, Hee Young A1 Kang, Hyoung Jin A1 Kook, Hoon A1 Kim, Seon Young A1 Kim, Soo-Jeong A1 Kim, Inho A1 Kim, Ji Yoon A1 Kim, Hawk A1 Park, Kyung Duki A1 Park, Kyung Bae A1 Park, Meerim A1 Park, Sang Kyu A1 Park, Eun Sil A1 Park, Jeong-A A1 Park, Jun Eun A1 Park, Ji Kyoung A1 Baek, Hee Jo A1 Seo, Jeong Ho A1 Shim, Ye Jee A1 Ahn, Hyo Seop A1 Yoo, Keon Hee A1 Yoon, Hoi Soo A1 Won, Young-Woong A1 Lee, Kun Soo A1 Lee, Kwang Chul A1 Lee, Mee Jeong A1 Lee, Sun Ah A1 Lee, Jun Ah A1 Lee, Jae Min A1 Lee, Jae Hee A1 Lee, Ji Won A1 Lim, Young Tak A1 Jung, Hyun Joo A1 Chueh, Hee Won A1 Choi, Eun Jin A1 Jung, Hye Lim A1 Kim, Ju Han A1 Lee, Dong Soon PB BioMed Central YR 2019 K1 Hereditary spherocytosis K1 RBC membrane disorder K1 Molecular diagnosis JF Orphanet Journal of Rare Diseases. 14(1):114 LK http://hdl.handle.net/10371/156024 DO http://hdl.handle.net/10371/156024 SF ELIB - SuUB Bremen
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