TY - JOUR
T1 - Gingival fibromatosis with sensorineural hearing loss
T2 - An autosomal dominant trait
AU - Hartsfield, J. K.
AU - Bixler, D.
AU - Hazen, R. H.
PY - 1985
Y1 - 1985
N2 - Gingival fibromatosis is a heterogeneous entity that can occur both as a part of syndromes and as an isolated trait. We describe the second family with a rare, dominantly inherited syndrome of gingival fibromatosis and progressive sensorineural hearing loss.
AB - Gingival fibromatosis is a heterogeneous entity that can occur both as a part of syndromes and as an isolated trait. We describe the second family with a rare, dominantly inherited syndrome of gingival fibromatosis and progressive sensorineural hearing loss.
UR - https://www.scopus.com/pages/publications/0022413690
UR - https://www.scopus.com/inward/citedby.url?scp=0022413690&partnerID=8YFLogxK
U2 - 10.1002/ajmg.1320220323
DO - 10.1002/ajmg.1320220323
M3 - Article
C2 - 4061496
AN - SCOPUS:0022413690
SN - 0148-7299
VL - 22
SP - 623
EP - 627
JO - American Journal of Medical Genetics
JF - American Journal of Medical Genetics
IS - 3
ER -