Original language | English |
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Pages (from-to) | 2762-2767 |
Journal | AM J MED GENET PART A |
Volume | 152A |
Issue number | 11 |
DOIs | |
Publication status | Published - 2010 |
Phenotypic variability of a deletion and duplication 6q16.1 → q21 due to a paternal balanced ins(7;6)(p15;q16.1q21).
Ana Spreiz, Doris Müller, Sibylle Zotter, Ursula Albrecht, Matthias Baumann, Christine Fauth, Martin Erdel, Johannes Zschocke, Gerd Utermann, Dieter Kotzot
Research output: Contribution to journal › Case report › peer-review
20
Citations
(Web of Science)