Literature DB >> 14130237

HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES.

P F LABAND, G HABIB, G S HUMPHREYS.   

Abstract

Entities:  

Keywords:  ABNORMALITIES; ADOLESCENCE; CHILD; EAR, EXTERNAL; FIBROMA; GENETICS, HUMAN; GINGIVA; HYPERTROPHY AND HYPERPLASIA; NEGROES; NOSE; PATHOLOGY; RADIOGRAPHY; SKELETON; SPLENOMEGALY; WEST INDIES

Mesh：

Year:  1964        PMID： 14130237     DOI： 10.1016/0030-4220(64)90506-7

Source DB:  PubMed          Journal:  Oral Surg Oral Med Oral Pathol        ISSN： 0030-4220


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  15 in total

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Authors:  Christiane K Bauer; Pauline E Schneeberger; Fanny Kortüm; Janine Altmüller; Fernando Santos-Simarro; Laura Baker; Jennifer Keller-Ramey; Susan M White; Philippe M Campeau; Karen W Gripp; Kerstin Kutsche
Journal:  Am J Hum Genet       Date:  2019-05-30       Impact factor: 11.025

2.  A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities.

Authors:  J P Fryns; F Moerman; P Goddeeris; C Bossuyt; H Van den Berghe
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

3.  Gene expression profiling and bioinformatics analysis of hereditary gingival fibromatosis.

Authors:  Lei Fang; Yu Wang; Xuejun Chen
Journal:  Biomed Rep       Date:  2017-12-15

4.  Hereditary gingival fibromatosis in children: a systematic review of the literature.

Authors:  Eirini Boutiou; Ioannis A Ziogas; Dimitrios Giannis; Aikaterini-Elisavet Doufexi
Journal:  Clin Oral Investig       Date:  2020-11-13       Impact factor: 3.573

5.  Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21.

Authors:  T C Hart; D Pallos; D W Bowden; J Bolyard; M J Pettenati; J R Cortelli
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

6.  A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15.

Authors:  Yufei Zhu; Wenxia Zhang; Zhenghao Huo; Yi Zhang; Yu Xia; Bo Li; Xiangyin Kong; Landian Hu
Journal:  Hum Genet       Date:  2006-10-31       Impact factor: 4.132

Review 7.  The Coffin-Siris syndrome. A report of four cases and review of the literature.

Authors:  J Lucaya; J A Garcia-Conesa; J M Bosch-Banyeras; G Pons-Peradejordi
Journal:  Pediatr Radiol       Date:  1981

8.  'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband Syndromes.

Authors:  Nuria C Bramswig; C W Ockeloen; J C Czeschik; A J van Essen; R Pfundt; J Smeitink; B T Poll-The; H Engels; T M Strom; D Wieczorek; T Kleefstra; H-J Lüdecke
Journal:  Hum Genet       Date:  2015-08-12       Impact factor: 4.132

Review 9.  Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.

Authors:  Xue Gao; Pu Dai; Yong-Yi Yuan
Journal:  Hum Genet       Date:  2021-07-07       Impact factor: 4.132

10.  Hereditary gingival fibromatosis.

Authors:  Prasad Vijayrao Dhadse; Ramareddy Krishnarao Yeltiwar; Prashant K Pandilwar; Suchitra R Gosavi
Journal:  J Indian Soc Periodontol       Date:  2012-10
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