Miriam Elbracht
0000-0001-5088-1369
5 papers found
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Germline variants in DNA repair genes, including BRCA1/2, may cause familial myeloproliferative neoplasms
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation
Inherited cases of CNOT3 ‐associated Intellectual Developmental Disorder with Speech Delay, Autism, and Dysmorphic Facies
Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients
Molecular and clinical studies in 8 patients with Temple syndrome
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