Items where Author is "Guleria, Vishal Singh"
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Article

Upadhyai, Priyanka and Radhakrishnan, Periyasamy and Guleria, Vishal Singh and Kausthubham, Neethukrishna and Nayak, Shalini S and Girisha, KM (2021) Biallelic deep intronic variant c.5457+81t>a in trip11 causes loss of function and results in achondrogenesis 1a. Human Mutation, 42 (8). pp. 1005-1014. ISSN 1059-7794

Somashekar, Puneeth H and Kaur, Parneet and Guleria, Vishal Singh and Rajagopal, KV and Girisha, KM and Stephen, Joshi and Upadhyai, Priyanka and Shukla, Anju (2021) Bi-allelic missense variant, p.Ser35Leu in EXOSC1 is associated with pontocerebellar hypoplasia. Clinical Genetics, 99 (4). pp. 594-600. ISSN 0009-9163

Upadhyai, Priyanka and Guleria, Vishal Singh and Udupa, Prajna (2020) Characterization of primary cilia features reveal cell-type specific variability in in vitro models of osteogenic and chondrogenic differentiation. PeerJ. pp. 1-25. ISSN 2167-8359

Upadhyai, Priyanka and Guleria, Vishal Singh and Udupa, Prajna (2020) Characterization of primary cilia features reveal cell-type specific variability in in vitro models of osteogenic and chondrogenic differentiation. PeerJ, 8 (e9799). pp. 1-25. ISSN 2167-8359

Upadhyai, Priyanka and Guleria, Vishal Singh and Girisha, KM and Shukla, Anju (2020) Recurrent 1q21.1 deletion syndrome: report on variable expression, nonpenetrance and review of literature. Clinical Dysmorphology, 29 (3). pp. 127-131. ISSN 0962-8827

This list was generated on Mon Jan 17 05:15:09 2022 UTC.