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

Coci, Emanuele G; Koehler, Udo; Liehr, Thomas; Stelzner, Armin; Fink, Christian; Langen, Hendrik; Riedel, Joachim.

Afiliación

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 en En | MEDLINE | ID: mdl-33750428

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Cytogenet Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

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