Genetic study on developmental dysplasia of the hip
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Biochemistry,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2362.2012.02682.x/fullpdf
Reference46 articles.
1. A two-locus model for non-syndromic congenital dysplasia of the hip (CDH);Sollazzo;Ann Hum Genet,2000
2. Congenital dislocation of the hip: the results of conservative treatment;Wilkinson;J Bone Joint Surg Br,1960
3. Persistent Joint Laxity and Congenital Dislocation of the Hip;Carter;J Bone Joint Surg Br,1964
4. Report of the delegation of clinical geneticists to China, Spring 1986;Laurence;Biol Soc,1987
5. Hip dysplasia: a significant risk factor for the development of hip osteoarthritis. A cross-sectional survey;Jacobsen;Rheumatology (Oxford),2005
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1. A Novel Heterozygous Missense Variant inParathyroid Hormone 1is Related to the Occurrence of Developmental Dysplasia of the Hip;Genetic Testing and Molecular Biomarkers;2023-03-01
2. Developmental dysplasia of the hip: A systematic review of susceptibility genes and epigenetics;Gene;2023-02
3. Case report: genetic analysis of a child with 18q deletion syndrome and developmental dysplasia of the hip;BMC Medical Genomics;2022-09-19
4. Heterozygous LRP1 deficiency causes developmental dysplasia of the hip by impairing triradiate chondrocytes differentiation due to inhibition of autophagy;Proceedings of the National Academy of Sciences;2022-09-06
5. Congenital dislocation of the hip – theories, etiological and predisposing factors (risk factors);Сибирский научный медицинский журнал;2022-08-27
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