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- Text 3
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- Abdalla, Ebtesam
- Alawi, Malik 3
- Kutsche, Kerstin 3
- Holling, Tess 2
- Abdelrazek, Ibrahim M. 1
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- Englisch 3
3 Einträge gefunden
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Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome-1 in two new patients with the same homozygous TMCO1 variant and review of the literature
- Abdelrazek, Ibrahim M.
- Holling, Tess
- Harms, Frederike Leonie
- Alawi, Malik
- Omar, Tarek
- Abdalla, Ebtesam
- Kutsche, Kerstin
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Cardiofacioneurodevelopmental syndrome: Report of a novel patient and expansion of the phenotype
2022 - Forschungsinformationssystem des UKE - frei zugänglich -
Clinically Relevant KCNQ1 Variants Causing KCNQ1-KCNE2 Gain-of-Function Affect the Ca2+ Sensitivity of the Channel
- Bauer, Christiane K
- Holling, Tess
- Horn, Denise
- Laço, Mário Nôro
- Abdalla, Ebtesam
- Omar, Omneya Magdy
- Alawi, Malik