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 journalCase reportpeer-review

20 Citations (Web of Science)
Original languageEnglish
Pages (from-to)2762-2767
JournalAM J MED GENET PART A
Volume152A
Issue number11
DOIs
Publication statusPublished - 2010

Cite this