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Expanding the spectrum of SMAD3‐related phenotypes to agnathia‐otocephaly by Nicole Meier, Elisabeth Bruder, Peter Miny, Sevgi Tercanli, Isabel Filges
Published 2020-04-01
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Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies by Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman, Melike Kirgiz, Tahir Dehgan, Tugba Kalayci, Bilge Ozsait Selcuk, Peter Miny, Atil Yuksel
Published 2022-12-01
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