|Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion|
E Klopocki, S Lohan, SC Doelken, S Stricker, CW Ockeloen, ...
Journal of medical genetics 49 (2), 119-125, 2012
|Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia|
A Dalal, SL Bhavani G, PP Togarrati, T Bierhals, MR Nandineni, S Danda, ...
American Journal of Medical Genetics Part A 158 (11), 2820-2828, 2012
|Congenital pseudarthrosis of the tibia treated with intramedullary rodding and cortical bone grafting: a follow-up study at skeletal maturity|
H Shah, SN Doddabasappa, B Joseph
Journal of Pediatric Orthopaedics 31 (1), 79-88, 2011
|Management of severe crouch gait in children and adolescents with cerebral palsy|
B Joseph, K Reddy, RA Varghese, H Shah, SN Doddabasappa
Journal of Pediatric Orthopaedics 30 (8), 832-839, 2010
|Congenital pseudarthrosis of the tibia: management and complications|
H Shah, M Rousset, F Canavese
Indian journal of orthopaedics 46 (6), 616, 2012
|Perthes disease: evaluation and management|
Orthopedic Clinics 45 (1), 87-97, 2014
|Effect of prophylactic trochanteric epiphyseodesis in older children with Perthes' disease|
H Shah, ND Siddesh, B Joseph, SN Nair
Journal of Pediatric Orthopaedics 29 (8), 889-895, 2009
|Mutations in patients with osteogenesis imperfecta from consanguineous Indian families|
J Stephen, KM Girisha, A Dalal, A Shukla, H Shah, P Srivastava, U Kornak, ...
European journal of medical genetics 58 (1), 21-27, 2015
|Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly|
E Klopocki, C Kähler, N Foulds, H Shah, B Joseph, H Vogel, S Lüttgen, ...
European journal of human genetics 20 (6), 705-708, 2012
|GALNS mutations in Indian patients with mucopolysaccharidosis IVA|
AM Bidchol, A Dalal, H Shah, S Nampoothiri, M Kabra, N Gupta, S Danda, ...
American Journal of Medical Genetics Part A 164 (11), 2793-2801, 2014
|Congenital posteromedial bowing of the tibia: a retrospective analysis of growth abnormalities in the leg|
HH Shah, SN Doddabasappa, B Joseph
Journal of Pediatric Orthopaedics B 18 (3), 120-128, 2009
|Pre-axial mirror polydactyly associated with tibial deficiency: a study of the patterns of skeletal anomalies of the foot and leg|
R Verghese, H Shah, G Rebello, B Joseph
Journal of children's orthopaedics 1 (1), 49-54, 2007
|Clinical utility of fetal autopsy and its impact on genetic counseling|
SS Nayak, A Shukla, L Lewis, R Kadavigere, M Mathew, PK Adiga, ...
Prenatal diagnosis 35 (7), 685-691, 2015
|Mutation spectrum of COL1A1 and COL1A2 genes in Indian patients with osteogenesis imperfecta|
J Stephen, A Shukla, A Dalal, KM Girisha, H Shah, N Gupta, M Kabra, ...
American journal of medical genetics Part A 164 (6), 1482-1489, 2014
|Environmental tobacco and wood smoke increase the risk of Legg-Calvé-Perthes disease|
AB Daniel, H Shah, A Kamath, V Guddettu, B Joseph
Clinical Orthopaedics and Related Research® 470 (9), 2369-2375, 2012
|Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy|
GSL Bhavani, H Shah, A Shukla, N Gupta, K Gowrishankar, AP Rao, ...
American Journal of Medical Genetics Part A 170 (2), 410-417, 2016
|Novel and recurrent mutations in WISP3 and an atypical phenotype|
GSL Bhavani, H Shah, AB Dalal, A Shukla, S Danda, S Aggarwal, ...
American Journal of Medical Genetics, Part A 167 (10), 2481-2484, 2015
|Recurrent and novel GLB1 mutations in India|
AM Bidchol, A Dalal, R Trivedi, A Shukla, S Nampoothiri, VH Sankar, ...
Gene 567 (2), 173-181, 2015
|Quantitative measures for evaluating the radiographic outcome of Legg-Calvé-Perthes disease|
H Shah, ND Siddesh, H Pai, S Tercier, B Joseph
JBJS 95 (4), 354-361, 2013
|A novel mutation (g. 106737G> T) in zone of polarizing activity regulatory sequence (ZRS) causes variable limb phenotypes in Werner mesomelia|
KM Girisha, AM Bidchol, PS Kamath, KH Shah, GR Mortier, S Mundlos, ...
American Journal of Medical Genetics Part A 164 (4), 898-906, 2014