Single central incisor in familial holoprosencephaly
- 1 June 1984
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 104 (6) , 877-880
- https://doi.org/10.1016/s0022-3476(84)80485-0
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter→q32:)]American Journal of Medical Genetics, 1983
- The dup(3)(p25 → pter) syndrome: A case with holoprosencephalyAmerican Journal of Medical Genetics, 1983
- Solitary central maxillary incisor associated with precocious puberty and hypothalamic hamartomaThe Journal of Pediatrics, 1982
- An update on the holoprosencephalic disordersThe Journal of Pediatrics, 1982
- Holoprosencephaly and endocrine dysgenesis in brothersAmerican Journal of Medical Genetics, 1980
- Congenitally missing maxillary central incisorOral Surgery, Oral Medicine, Oral Pathology, 1979
- Solitary maxillary central incisor and normal statureOral Surgery, Oral Medicine, Oral Pathology, 1978
- Solitary maxillary central incisor and short statureThe Journal of Pediatrics, 1977
- Congenital single incisorOral Surgery, Oral Medicine, Oral Pathology, 1974
- Familial holoprosencephaly with endocrine dysgenesisThe Journal of Pediatrics, 1968