Hypertrichosis terminalis, gingival hyperplasia, and a characteristic face: A new distinct entity
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference13 articles.
1. A new case of Ambras syndrome associated with a paracentric inversion (8)(q12;q22);Balducci;Clin Genet,1998
2. Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2;q22);Baumeister;Clin Genet,1993
3. Congenital hypertrichosis lanuginose;Beighton;Arch Dermatol,1970
4. Julia Pastrana, the nondescript: an example of congenital, generalized hypertrichosis terminals with gingival hyperplasia;Bondeson;Am J Med Genet,1993
5. A distinct osteochondrodysplasia with hypertrichosis-individualization of a probable autosomal recessive entity;Cantú;Hum Genet,1982
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2. Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosis;Clinical and Experimental Dermatology;2022-06-01
3. Hyaline fibromatosis syndrome: a case presenting with gingival enlargement as the only clinical manifestation and a report of two new mutations in the ANTXR2 gene;BMC Oral Health;2021-10-09
4. Hereditary gingival fibromatosis associated with the missense mutation of the KCNK4 gene;Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology;2021-06
5. Generalized hypertrichosis syndromes in Mexico;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2020-12
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