Author/Creator: Shah, Krati - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Shah, Krati

1. C‐reactive protein gene polymorphisms (rs1205) in Asian Indian patients with Takayasu arteritis: Associations and phenotype correlations. (11th October 2017)

Authors:: Nair, Aswin M.; Goel, Ruchika; Hindhumati, Mohan; Shah, Krati; Chandana, Puneet; Jayaseelan, Visalakshi; Jayakanthan, Kabeerdoss; Joseph, George; Danda, Sumita; Danda, Debashish
Journal:: International journal of rheumatic diseases
Issue:: Volume 21:Number 3(2018)
Page Start:: 732
Record Type:: Journal Article
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2. GM2 gangliosidosis AB variant: novel mutation from India – a case report with a review. Issue 1 (December 2016)

Authors:: Sheth, Jayesh; Datar, Chaitanya; Mistri, Mehul; Bhavsar, Riddhi; Sheth, Frenny; Shah, Krati
Journal:: BMC pediatrics
Issue:: Volume 16:Issue 1(2016)
Page Start:: 1
Record Type:: Journal Article
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3. Novel LINS1 missense mutation in a family with non‐syndromic intellectual disability. Issue 4 (9th February 2017)

Authors:: Sheth, Jayesh; Ranjan, Gyan; Shah, Krati; Bhavsar, Riddhi; Sheth, Frenny
Journal:: American journal of medical genetics
Issue:: Volume 173:Issue 4(2017)
Page Start:: 1041
Record Type:: Journal Article
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4. Novel mutations in the LRP5 gene in patients with Osteoporosis‐pseudoglioma syndrome. Issue 12 (21st October 2017)

Authors:: Pekkinen, Minna; Grigelioniene, Giedre; Akin, Leyla; Shah, Krati; Karaer, Kadri; Kurtoğlu, Selim; Ekbote, Alka; Aycan, Zehra; Sağsak, Elif; Danda, Sumita; Åström, Eva; Mäkitie, Outi
Journal:: American journal of medical genetics
Issue:: Volume 173:Issue 12(2017)
Page Start:: 3132
Record Type:: Journal Article
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5. Pulmonary manifestations in Niemann-Pick type C disease with mutations in NPC2 gene: case report and review of literature. Issue 1 (December 2017)

Authors:: Sheth, Jayesh; Joseph, Jijo; Shah, Krati; Muranjan, Mamta; Mistri, Mehul; Sheth, Frenny
Journal:: BMC medical genetics
Issue:: Volume 18:Issue 1(2017)
Page Start:: 1
Record Type:: Journal Article
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6. Whole exome sequencing reveals novel LEPR frameshift mutation in severely obese children from Western India. Issue 7 (8th May 2019)

Authors:: Bhatt, Arpan; Purani, Charul; Bhargava, Poonam; Patel, Komal; Agarbattiwala, Tanvi; Puvar, Apurvasinh; Shah, Krati; Joshi, Chaitanya G.; Dhamecha, Nidhi; Prabhakar, Mukund; Joshi, Madhvi
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 7:Issue 7(2019)
Page Start:: n/a
Record Type:: Journal Article
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