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K M Girisha

Showing results (11-20 of 42) with videos related to

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Clinical Genetics|March 10, 2017
Second family provides further evidence for causation of Steel syndrome by biallelic mutations in COL27A1S Kotabagi, H Shah, A Shukla, et al.
Genetic Counseling (Geneva, Switzerland)|August 5, 2010
Balanced translocation in mother leading to interchange trisomy 21?K M Girisha, M Rajasekhar, P M Gopinath, et al.
Journal of Postgraduate Medicine|October 12, 2010
Preimplantation diagnosis of genetic diseasesS K Adiga, G Kalthur, P Kumar, et al.
Indian Pediatrics|September 5, 2006
S252W mutation in Indian patients of Apert syndromeK M Girisha, Shubha R Phadke, Faisal Khan, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Massive cranial osteolysis, skin changes, growth retardation and developmental delay: Gorham syndrome with systemic manifestations?K M Girisha, H K Ganesh, Lakshmi Rao, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Severe rhizomelic chondrodysplasia punctata in a fetus due to maternal mixed connective tissue disorderS S Nayak, P K Adiga, L Rai, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
ALOBAR HOLOPROSENCEPHALY, CLEFT LIP/PALATE, URORECTAL SEPTUM MALFORMATION SEQUENCE AND CONGENITAL PERINEAL HERNIA IN A FETUSK M Girisha, S S Nayak, A Shukla, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
A de novo translocation of chromosomes 1 and 2 in an 18 year old boy with syndromic mental retardationJ Neetha, K M Girisha, P M Gopinath, et al.
Indian Pediatrics|November 15, 2011
Profile of patients with Von Gierke disease from IndiaParag M Tamhankar, Vijayraju Boggula, K M Girisha, et al.
Journal of Children'S Orthopaedics|August 2, 2013
Loss of a condyle of the femur or tibia following septic arthritis in infancy: problems of management and testing of a hypothesis of pathogenesisStéphane Tercier, N D Siddesh, Hitesh Shah, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Clinical Genetics|March 10, 2017
Second family provides further evidence for causation of Steel syndrome by biallelic mutations in COL27A1S Kotabagi, H Shah, A Shukla, et al.
Genetic Counseling (Geneva, Switzerland)|August 5, 2010
Balanced translocation in mother leading to interchange trisomy 21?K M Girisha, M Rajasekhar, P M Gopinath, et al.
Journal of Postgraduate Medicine|October 12, 2010
Preimplantation diagnosis of genetic diseasesS K Adiga, G Kalthur, P Kumar, et al.
Indian Pediatrics|September 5, 2006
S252W mutation in Indian patients of Apert syndromeK M Girisha, Shubha R Phadke, Faisal Khan, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Massive cranial osteolysis, skin changes, growth retardation and developmental delay: Gorham syndrome with systemic manifestations?K M Girisha, H K Ganesh, Lakshmi Rao, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Severe rhizomelic chondrodysplasia punctata in a fetus due to maternal mixed connective tissue disorderS S Nayak, P K Adiga, L Rai, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
ALOBAR HOLOPROSENCEPHALY, CLEFT LIP/PALATE, URORECTAL SEPTUM MALFORMATION SEQUENCE AND CONGENITAL PERINEAL HERNIA IN A FETUSK M Girisha, S S Nayak, A Shukla, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
A de novo translocation of chromosomes 1 and 2 in an 18 year old boy with syndromic mental retardationJ Neetha, K M Girisha, P M Gopinath, et al.
Indian Pediatrics|November 15, 2011
Profile of patients with Von Gierke disease from IndiaParag M Tamhankar, Vijayraju Boggula, K M Girisha, et al.
Journal of Children'S Orthopaedics|August 2, 2013
Loss of a condyle of the femur or tibia following septic arthritis in infancy: problems of management and testing of a hypothesis of pathogenesisStéphane Tercier, N D Siddesh, Hitesh Shah, et al.
Pageof 5