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PubPharm (57)
1
The potential influence of GSTT1 null genetic polymorphism on coronary artery disease : A pilot study in a South Indian cohort
enthalten in:
Indian heart journal
| 2024
von
Rajamuthiah, P.
|
Krishnan B B, S.
|
Antony, S.
| +1
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2
Risk association of the nitric oxide synthase VNTR intron 4 a/b variant with diabetic nephropathy - a pilot study
enthalten in:
Nucleosides, nucleotides & nucleic acids
| 2024
von
Moorthy, S.
|
Koshy, T.
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3
Mercaptopurine induced myelosuppression in a child with a NUDT15 rs116855232 homozygous variant
enthalten in:
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
| 2023
von
Gupta, N.
|
Magatha, L.
|
Jayaraman, D.
| +3
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4
Case Report : A Disease Phenotype of Rett Syndrome and Neurofibromatosis Resulting from A Bilocus Variant Combination
enthalten in:
Journal of autism and developmental disorders
| 2023
von
Narasimhan, U.
|
Janakiraman, A.
|
Puskur, D.
| +3
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5
Candidate Gene Expression in Regional Population and Its Relevance for Radiation Triage
enthalten in:
Cytogenetic and genome research
| 2023
von
Kannan, N.
|
Koshy, T.
|
Raavi, V.
| +6
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6
Case Report: A Disease Phenotype of Rett Syndrome and Neurofibromatosis Resulting from A Bilocus Variant Combination
enthalten in:
Journal of autism and developmental disorders
| 2022
von
Narasimhan, U.
|
Janakiraman, A.
|
Puskur, D.
| +3
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7
Burden of Type 2 Diabetes and Associated Cardiometabolic Traits and Their Heritability Estimates in Endogamous Ethnic Groups of India : Findings From the INDIGENIUS Consortium
enthalten in:
Frontiers in endocrinology
| 2022
von
Venkatesan, V.
|
Lopez-Alvarenga, J.
|
Arya, R.
| +31
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8
Cortisol and polycystic ovarian syndrome - a systematic search and meta-analysis of case-control studies
enthalten in:
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology
| 2021
von
Benjamin, J.
|
Kuppusamy, M.
|
Koshy, T.
| +2
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9
Blast size-specific flowcytometric ploidy assessment using FxCycleTM Violet dye and its correlation with conventional cytogenetic ploidy in pediatric precursor B-lineage acute lymphoblastic leukemia patients
enthalten in:
International journal of laboratory hematology
| 2021
von
Bommannan, K.
|
Arumugam, J.
|
Koshy, T.
| +3
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10
Utility of clinical exome sequencing in the evaluation of neonates with suspected genetic condition - An observational study from tertiary neonatal care unit in South India
enthalten in:
European journal of medical genetics
| 2021
von
Usha Devi, R.
|
Thinesh Kumar, J.
|
Jan, S.
| +4
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57
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Indian journal of pediatrics
4
Journal of assisted reproduction and genetics
4
Laboratory medicine
4
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3
Cytogenetic and genome research
3
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2
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2
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The journal of pediatric endocrinology and meta...
1
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1
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1
Frontiers in endocrinology
1
Gynecological endocrinology : the official jour...
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Indian heart journal
1
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1
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Indian journal of hematology and blood transfusion
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Thema
32
Journal Article
8
Single nucleotide polymorphism
7
Case Reports
4
Cytogenetics
4
Deoxyribonucleic acid
4
Fetal genotypes
4
Folate metabolism
4
Idiopathic recurrent spontaneous abortion
4
Logistic regression
4
Matrix metalloproteinase
4
Sanger sequencing
3
Acute lymphoblastic leukemia
3
India
3
Karyotype
3
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3
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3
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3
haplotype analysis
3
multiplex ligation-dependent probe amplification
2
Bacopa monniera
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Erscheinungszeitraum
19
2020-
36
2010-2019
2
2000-2009
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