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Your search keyword '"Henderson, Robert H."' showing total 7 results

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7 results on '"Henderson, Robert H."'

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1. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

2. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

3. Immediate Sequential Bilateral Pediatric Vitreoretinal Surgery: An International Multicenter Study

4. RDH12 retinopathy: novel mutations and phenotypic description

5. Novel mutations in MERTK associated with childhood onset rod-cone dystrophy

6. Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humans

7. A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction

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