Literature DB >> 14496532

Osteopetrosis: review of dominant cases and frequency in a Brazilian state.

F M SALZANO.   

Abstract

Entities:  

Keywords:  OSTEOPETROSIS

Mesh：

Year:  1961        PMID： 14496532     DOI： 10.1017/s1120962300016954

Source DB:  PubMed          Journal:  Acta Genet Med Gemellol (Roma)        ISSN： 0001-5660


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  6 in total

1.  Monogenic disorders.

Authors:  C O Carter
Journal:  J Med Genet       Date:  1977-10       Impact factor: 6.318

2.  Mapping of autosomal dominant osteopetrosis type II (Albers-Schönberg disease) to chromosome 16p13.3.

Authors:  O Bénichou; E Cleiren; J Gram; J Bollerslev; M C de Vernejoul; W Van Hul
Journal:  Am J Hum Genet       Date:  2001-07-23       Impact factor: 11.025

3.  Fractures in patients with osteopetrosis, insights from a single institution.

Authors:  Anuj Chawla; Ernest Beng Kee Kwek
Journal:  Int Orthop       Date:  2018-10-04       Impact factor: 3.075

4.  A Case of Autosomal Dominant Osteopetrosis Type 2 with a CLCN7 Gene Mutation

Authors:  Sol Kang; Young Kyung Kang; Jun Ah Lee; Dong Ho Kim; Jung Sub Lim
Journal:  J Clin Res Pediatr Endocrinol       Date:  2019-02-14

Review 5.  Friend or foe: high bone mineral density on routine bone density scanning, a review of causes and management.

Authors:  Celia L Gregson; Sarah A Hardcastle; Cyrus Cooper; Jonathan H Tobias
Journal:  Rheumatology (Oxford)       Date:  2013-02-27       Impact factor: 7.580

Review 6.  The Genetic Architecture of High Bone Mass.

Authors:  Celia L Gregson; Emma L Duncan
Journal:  Front Endocrinol (Lausanne)       Date:  2020-10-29       Impact factor: 5.555
  6 in total

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