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Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes.
Coci, Emanuele G; Koehler, Udo; Liehr, Thomas; Stelzner, Armin; Fink, Christian; Langen, Hendrik; Riedel, Joachim.
Affiliation
  • Coci EG; Center of Social Pediatrics and Pediatric Neurology, General Hospital of Celle, 29221, Celle, Germany. Emanuele.Coci@akh-celle.de.
  • Koehler U; Medizinisch Genetisches Zentrum, 80335, Munich, Germany.
  • Liehr T; Institute of Human Genetics, Friedrich Schiller University, Jena University Hospital, 07743, Jena, Germany.
  • Stelzner A; Center of Social Pediatrics and Pediatric Neurology, General Hospital of Celle, 29221, Celle, Germany.
  • Fink C; Department of Radiology, General Hospital of Celle, 29223, Celle, Germany.
  • Langen H; Center of Social Pediatrics and Pediatric Neurology, General Hospital of Celle, 29221, Celle, Germany.
  • Riedel J; Center of Social Pediatrics and Pediatric Neurology, General Hospital of Celle, 29221, Celle, Germany.
Mol Cytogenet ; 14(1): 17, 2021 Mar 09.
Article in En | MEDLINE | ID: mdl-33750428
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Full text: 1 Database: MEDLINE Language: En Journal: Mol Cytogenet Year: 2021 Type: Article Affiliation country: Germany
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Full text: 1 Database: MEDLINE Language: En Journal: Mol Cytogenet Year: 2021 Type: Article Affiliation country: Germany