Suchergebnisse - "Ha, Thuong T"

PubPharm (7)

1

Author Correction : Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

enthalten in: Nature medicine | 2024

von Byrne, A. | Arts, P. | Ha, T. | +129

ErratumFor: Nat Med. 2023 Jan;29(1):180-189. - PMID 36658419

2

Aicardi Syndrome Is a Genetically Heterogeneous Disorder

enthalten in: Genes | 2023

von Ha, T. | Burgess, R. | Newman, M. | +19

3

Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis

enthalten in: Neuromuscular disorders : NMD | 2023

von Ghaoui, R. | Ha, T. | Kerkhof, J. | +11

4

Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

enthalten in: Nature medicine | 2023

von Byrne, A. | Arts, P. | Ha, T. | +129

CommentIn: Nat Med. 2023 Jan;29(1):41-42. - PMID 36670297

5

Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disability

enthalten in: Human mutation | 2021

von Field, M. | Kumar, R. | Hackett, A. | +19

6

Different types of disease‐causing noncoding variants revealed by genomic and gene expression analyses in families with X‐linked intellectual disability

enthalten in: Human mutation | 2021

von Field, M. | Kumar, R. | Hackett, A. | +19

7

A mutation in COL4A2 causes autosomal dominant porencephaly with cataracts

enthalten in: American journal of medical genetics. Part A | 2016

von Ha, T. | Sadleir, L. | Mandelstam, S. | +4

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