Results 221 to 230 of about 10,658 (245)

Amelogenesis imperfecta:A Genetic Study

Human Heredity, 1988
The mode of inheritance and the clinical manifestations of amelogenesis imperfecta (AI) were studied in 51 families from the county of Västerbotten, northern Sweden. Autosomal dominant (AD) was the most probable mode of inheritance in 33 families, but X-linked dominant (XD) inheritance was a possible alternative in one family.
B, Bäckman, G, Holmgren
openaire   +2 more sources

Amelogenesis imperfecta

Universal Research Journal of Dentistry, 2012
Tofiq Bohra, MohammedAnwar Ul Haque Chand, Adwait Kulkarni, Aruna Tambuwala, Adwait Tembey   +4 more
openaire   +2 more sources

Amelogenesis imperfecta

Tandartspraktijk, 2017
Marcel Linssen, Hans van Pelt
openaire   +2 more sources

Amelogenesis imperfecta

European Journal of Oral Sciences, 2011
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Amelogenesis imperfecta

Tandartspraktijk, 2013
Khee Hian Phoa, Jacolien Wismeijer, Hans van Pelt   +2 more
openaire   +1 more source

amelogenesis, n.

2023
openaire   +1 more source

Amelogenesis imperfecta

Oral Surgery, Oral Medicine, Oral Pathology, 1975
Lj, Neceva, M, Mirceva
openaire   +3 more sources

Amelogenesis Imperfecta

2016
Michael Aldred, Anna Talacko, Netasha Steyn   +2 more
openaire   +1 more source

Alkaline phosphatase in amelogenesis

The Anatomical Record, 1949
G, BEVELANDER, P L, JOHNSON
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[Amelogenesis. I. Cellular aspects of amelogenesis].

L' Information dentaire, 1981
openaire   +1 more source