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Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: A case report

Document Type

Article

Author

Nistico, D.; D'Adamo, A.P.; Barbi, E.; Gasparini, P.; Cadenaro, M.; Guidolin, F.; Navarra, C.O.; Bobbo, M.; Magnolato, A.; Sirchia, F.; Giorgio, E.; Pivetta, B.

Source

In: BMC Pediatrics. (BMC Pediatrics, 9 May 2020, 20(1))

Subject

Language

English

ISSN

14712431

Online Access

Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Open Access (BioMed Central) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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