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Search Results - Neethukrishna, K
Search Results - Neethukrishna, K
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Autosomal recessive spinocerebellar ataxia 20: Report of a new patient and review of literature
by
Shukla, Anju
,
Upadhyai, Priyanka
,
Shah, Jhanvi
,
Neethukrishna, K
,
Bielas, Stephanie
,
Girisha, K.M
Published in
European journal of medical genetics
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Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies
by
Hammarsjö, A
,
Wang, Z
,
Vaz, R
,
Taylan, F
,
Sedghi, M
,
Girisha, K M
,
Chitayat, D
,
Neethukrishna, K
,
Shannon, P
,
Godoy, R
,
Gowrishankar, K
,
Lindstrand, A
,
Nasiri, J
,
Baktashian, M
,
Newton, P T
,
Guo, L
,
Hofmeister, W
,
Pettersson, M
,
Chagin, A S
,
Nishimura, G
,
Yan, L
,
Matsumoto, N
,
Nordgren, A
,
Miyake, N
,
Grigelioniene, G
,
Ikegawa, S
Published in
Scientific reports
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Proteomic analysis of a compatible interaction between sugarcane and Sporisorium scitamineum
by
Barnabas, Leonard
,
Ashwin, N. M. R.
,
Kaverinathan, K.
,
Trentin, Anna Rita
,
Pivato, Micaela
,
Sundar, A. Ramesh
,
Malathi, P.
,
Viswanathan, R.
,
Rosana, O. B.
,
Neethukrishna, K.
,
Carletti, Paolo
,
Arrigoni, Giorgio
,
Masi, Antonio
,
Agrawal, Ganesh Kumar
,
Rakwal, Randeep
Published in
Proteomics (Weinheim)
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Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia
by
Chang, Hae Ryung
,
Cho, Sung Yoon
,
Lee, Jae Hoon
,
Lee, Eunkyung
,
Seo, Jieun
,
Lee, Hye Ran
,
Cavalcanti, Denise P.
,
Mäkitie, Outi
,
Valta, Helena
,
Girisha, Katta M.
,
Lee, Chung
,
Neethukrishna, Kausthubham
,
Bhavani, Gandham S.
,
Shukla, Anju
,
Nampoothiri, Sheela
,
Phadke, Shubha R.
,
Park, Mi Jung
,
Ikegawa, Shiro
,
Wang, Zheng
,
Higgs, Martin R.
,
Stewart, Grant S.
,
Jung, Eunyoung
,
Lee, Myeong-Sok
,
Park, Jong Hoon
,
Lee, Eun A.
,
Kim, Hongtae
,
Myung, Kyungjae
,
Jeon, Woosung
,
Lee, Kyoungyeul
,
Kim, Dongsup
,
Kim, Ok-Hwa
,
Choi, Murim
,
Lee, Han-Woong
,
Kim, Yonghwan
,
Cho, Tae-Joon
Published in
American journal of human genetics
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Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing
by
Nayak, Shalini S
,
Schneeberger, Pauline E
,
Patil, Siddaramappa J
,
Arun, Karegowda M
,
Suresh, Pujar V
,
Kiran, Viralam S
,
Siddaiah, Sateesh
,
Maiya, Shreesha
,
Venkatachalagupta, Shrikanth K
,
Kausthubham, Neethukrishna
,
Kortüm, Fanny
,
Rau, Isabella
,
Wey-Fabrizius, Alexandra
,
Van Den Heuvel, Lotte
,
Meester, Josephina
,
Van Laer, Lut
,
Shukla, Anju
,
Loeys, Bart
,
Girisha, Katta M
,
Kutsche, Kerstin
Published in
Scientific reports
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Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities
by
Kaur, Parneet
,
Rosario, Michelle C
,
Hebbar, Malavika
,
Sharma, Suvasini
,
Kausthubham, Neethukrishna
,
Nair, Karthik
,
A, Shrikiran
,
Bhat Y, Ramesh
,
Lewis, Leslie Edward S
,
Nampoothiri, Sheela
,
Patil, Siddaramappa J
,
Suresh, Narayanaswami
,
Bijarnia Mahay, Sunita
,
Dua Puri, Ratna
,
Pai, Shivanand
,
Kaur, Anupriya
,
KC, Rakshith
,
Kamath, Nutan
,
Bajaj, Shruti
,
Kumble, Ali
,
Shetty, Rajesh
,
Shenoy, Rathika
,
Kamate, Mahesh
,
Shah, Hitesh
,
Muranjan, Mamta N
,
BL, Yatheesha
,
Avabratha, K Shreedhara
,
Subramaniam, Girish
,
Kadavigere, Rajagopal
,
Bielas, Stephanie
,
Girisha, Katta Mohan
,
Shukla, Anju
Published in
Clinical genetics
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