Literature DB >> 4327157

Manifestations of genetic diseases in the human pulp.

C J Witkop.   

Abstract

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Year:  1971        PMID： 4327157     DOI： 10.1016/0030-4220(71)90232-5

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


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  21 in total

Review 1.  Review of the dental implications of X-linked hypophosphataemic rickets (XLHR).

Authors:  Martin M I Sabandal; Peter Robotta; Sebastian Bürklein; Edgar Schäfer
Journal:  Clin Oral Investig       Date:  2015-02-13       Impact factor: 3.573

2.  Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.

Authors:  Jung-Wook Kim; Jan C-C Hu; Jae-Il Lee; Sung-Kwon Moon; Young-Jae Kim; Ki-Taeg Jang; Sang-Hoon Lee; Chong-Chul Kim; Se-Hyun Hahn; James P Simmer
Journal:  Hum Genet       Date:  2004-12-08       Impact factor: 4.132

3.  Hereditary dentine dysplasias: terminology in the context of osteogenesis imperfecta.

Authors:  M Chetty; T Roberts; L X G Stephen; P Beighton
Journal:  Br Dent J       Date:  2016-12-09       Impact factor: 1.626

4.  Non syndromic familial bilateral decidious taurodontism - a first case report.

Authors:  Antarmayee Panigrahi; Rajat G Panigrahi; Srilatha K T; Ruchi Bhuyan; Sanat K Bhuyan
Journal:  J Clin Diagn Res       Date:  2014-12-05

5.  Taurodontism and Klinefelter's syndrome.

Authors:  Y Komatz; T Tomoyoshi; O Yoshida; A Fujimoto; K Yoshitake
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

6.  Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II.

Authors:  B Malmgren; S Lindskog; A Elgadi; S Norgren
Journal:  Hum Genet       Date:  2004-02-03       Impact factor: 4.132

7.  Taurodontism in deciduous molars.

Authors:  Yash Bafna; H V Kambalimath; Vishal Khandelwal; Prathibha Nayak
Journal:  BMJ Case Rep       Date:  2013-06-03

8.  Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia.

Authors:  Serap Turan; Cumhur Aydin; Abdullah Bereket; Teoman Akcay; Tülay Güran; Betul Akmen Yaralioglu; Murat Bastepe; Harald Jüppner
Journal:  Bone       Date:  2009-09-29       Impact factor: 4.398

Review 9.  Taurodontism, an isolated trait associated with syndromes and X-chromosomal aneuploidy.

Authors:  M T Jaspers; C J Witkop
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

10.  A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family.

Authors:  Xianqin Zhang; Lanying Chen; Jingyu Liu; Zhen Zhao; Erjun Qu; Xiaotao Wang; Wei Chang; Chengqi Xu; Qing K Wang; Mugen Liu
Journal:  BMC Med Genet       Date:  2007-08-08       Impact factor: 2.103
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