Single mandibular incisor in a patient with del (18p) anomaly

Author:

Pfeiffer R. A.,Hertrich K.,Cohen M.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference15 articles.

1. A single maxillary central incisor in a girl with del (18p) syndrome;Aughton;J Med Genet,1991

2. Agnathia-holoprosencephaly: a developmental field complex involving face and brain. Report of 3 cases;Bixler;J Craniofac Genet Develop Biol,1985

3. Incisive superieure unique, hypopituitarisme et anomalie chromosomique monosomie 18p;Boudaillez;J Genet Hum,1983

4. Perspectives on holoprosencephaly. Part III. Spectra, distinctions, continuities and discontinuities;Cohen;Am J Med Genet,1989

5. 18p- syndrome with a single central maxillary incisor;Dolan;J Med Genet,1981

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1. Parental consanguinity a possible risk factor for tooth agenesis: A case series;International Journal of Oral Health Dentistry;2022-12-15

2. A patient with chromosome 18p deletion and congenital hypoglossia;Clinical Dysmorphology;2018-04

3. Agenesis of Permanent Mandibular Central Incisors: A Concordant Condition in Siblings;International Journal of Clinical Pediatric Dentistry;2016

4. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

5. Clinical and molecular characterization of individuals with 18p deletion: A genotype–phenotype correlation;American Journal of Medical Genetics Part A;2006

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