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Meindert Lamers Selected Research

Arhinia, choanal atresia, and microphthalmia

10/2019SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain.

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Meindert Lamers Research Topics

Disease

1Neoplasms (Cancer)
11/2021
1Arhinia, choanal atresia, and microphthalmia
10/2019
1Facioscapulohumeral Muscular Dystrophy
10/2019

Drug/Important Bio-Agent (IBA)

1DNA (Deoxyribonucleic Acid)IBA
11/2021
1Adenosine Triphosphatases (ATPase)IBA
10/2019
1Proteins (Proteins, Gene)FDA Link
10/2019