Single maxillary central incisor and coloboma in hypomelanosis of Ko

Author:

Bartholomew D. W.,Jabs E. W.,Levin L. S.,Ribovich R.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference11 articles.

1. Dental dysplasia in incontinentia pigmenti achromians (Ito), an unusual form;Browne;Br. Dent. J.,1976

2. 18p- Syndrome with a single central maxillary incisor;Dolan;J. Med. Genet.,1981

3. Focal Cerebral Atrophy in Incontinenta Pigmenti Achromians;Donat;Am. J. Dis. Child.,1980

4. Hamartoma-tous dental cusps in hypomelanosis oflto;Happle;Clin. Genet.,1982

5. Hypomelanosis of Ito associated with benign tumors and chromosomal abnormalities: a neurocutaneous syndrome;Ishikawa;J. Med. Genet.,1985

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1. Genetic Diseases;Periodontal Manifestations of Local and Systemic Diseases;2023

2. Hypomelanosis of Ito;Neurocutaneous Syndromes;2015

3. Dental findings and management in a child with hypomelanosis of Ito;Pediatric Dental Journal;2014-12

4. Haut und Zähne;Der Hautarzt;2009-06-20

5. Dental manifestations of dermatologic conditions;Journal of the American Academy of Dermatology;2009-02

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