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Preimplantation genetic diagnosis for mitochondrial DNA disorders: ethical guidance for clinical practiceSimultaneous mutation detection in 90 retinal disease genes in multiple patients using a custom-designed 300-kb retinal resequencing chip.Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotidesDefinition of subchromosomal intervals around the myotonic dystrophy gene region at 19qA patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2
P50
description
researcher ORCID ID = 0000-0003-1620-908X
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wetenschapper
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name
Bert Smeets
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Bert Smeets
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Bert Smeets
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Bert Smeets
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type
label
Bert Smeets
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Bert Smeets
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Bert Smeets
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Bert Smeets
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altLabel
B. Smeets
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prefLabel
Bert Smeets
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Bert Smeets
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Bert Smeets
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Bert Smeets
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P1153
35432038900
P19
P21
P31
P496
0000-0003-1620-908X
P569
1960-09-30T00:00:00Z
P734
P735
P7449
PRS1272615