Author

Melik Malek Khelifa

Observed name: Khelifa, Melik Malek

Institution: Medizinische Hochschule Hannover

Observed institution: Medizinische Hochschule Hannover

OpenAlex ID: A5092799396

Further delineation of the rare GDACCF (global developmental delay, absent or hypoplastic corpus callosum, dysmorphic facies syndrome): genotype and phenotype of 22 patients with ZNF148 mutations

2023 · Katalin Szakszon, Charles Marques Lourenco, et al. · Journal of Medical Genetics · 4

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND)

2026 · Sally Nijim, Mimi Kim, et al. · Genetics in Medicine · 1

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

2026 · Nijim, Sally, Kim, Mimi, et al. · Open Access CRIS of the University of Bern

Works count: 4

Citation count: 5

H-index: 1

I10-index: