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18
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Pubcomment Prop Sub 244 - Proposal to clarify OPTN policies.pdf
- Pubcomment Prop Sub 244 - Proposal to clarify OPTN policies
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10
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identification of an alu-repeat-mediated deletion of optn upstream region in a patient with a complex ocular phenotype.识别optn alu-repeat-mediated删除的上.pdf
- identification of an alu-repeat-mediated deletion of optn upstream region in a patient with a complex ocular phenotype.识别optn alu-repeat-mediated删除的上
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11
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optn policy regarding prioritization of patients with hepatopulmonary syndrome does it provide equitable organ allocation.pdf
- optn policy regarding prioritization of patients with hepatopulmonary syndrome does it provide equitable organ allocation
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16
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Multiple listing for pediatric heart transplantation in the USA Analysis of OPTN registry data from 1995 through 2009.pdf
- Multiple listing for pediatric heart transplantation in the USA Analysis of OPTN registry data from 1995 through 2009
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15
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Resource Utilization Associated with Procurement of Transplantable Organs from Donors that do not meet OPTN Eligible Death Criteria.pdf
- Resource Utilization Associated with Procurement of Transplantable Organs from Donors that do not meet OPTN Eligible Death Criteria
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16
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Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.pdf
- Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease
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22
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HLA Antigen Tables - OPTN.pdf
- HLA Antigen Tables - OPTN
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12
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The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes.pdf
- The majority of the genetic risk for Paget’s disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes
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44
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原发性开角型青光眼的遗传学调查与optn基因突变的研究.pdf
- 原发性开角型青光眼的遗传学调查与optn基因突变的研究,原发性青光眼,基因遗传学,基因突变,基因突变器,基因突变和基因重组,基因突变的特点,n2基因突变生化地雷,基因突变类型,egfr基因突变检测
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向豆丁求助：有没有optn?
