Suchergebnisse - "Miao, Mingzhu"

PubPharm (6)

1

Identification of a novel de novo PUF60 variant causing Verheij syndrome in a fetus

enthalten in: Gene | 2024

von Miao, M. | Wang, J. | Guo, C. | +3

2

A novel PKHD1 splicing variant identified in a fetus with autosomal recessive polycystic kidney disease

enthalten in: Frontiers in genetics | 2023

von Miao, M. | Feng, L. | Wang, J. | +4

3

Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation

enthalten in: BMC medical genomics | 2022

von Miao, M. | Lu, S. | Sun, X. | +5

4

Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation

enthalten in: BMC medical genomics | 2022

von Miao, M. | Lu, S. | Sun, X. | +5

5

Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation

enthalten in: BMC medical genomics | 2022

von Miao, M. | Lu, S. | Sun, X. | +5

6

Non-invasive prenatal detection of trisomy 21 by quantifying segmental duplication in maternal plasma with digital PCRElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ay00122j

enthalten in: Analytical methods | 2016

von Xu, S. | Zou, B. | Xiang, Z. | +5

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