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1دورية أكاديمية
المؤلفون: Jayesh Sheth, Aadhira Nair, Frenny Sheth, Manali Ajagekar, Tejasvi Dhondekar, Inusha Panigrahi, Ashish Bavdekar, Sheela Nampoothiri, Chaitanya Datar, Ajit Gandhi, Mamta Muranjan, Anupriya Kaur, Manisha Desai, Mehul Mistri, Chitra Patel, Premal Naik, Maulin Shah, Koumudi Godbole, Seema Kapoor, Neerja Gupta, Sunita Bijarnia-Mahay, Sandeep Kadam, Dhaval Solanki, Soham Desai, Anand Iyer, Ketan Patel, Harsh Patel, Raju C. Shah, Shalmi Mehta, Ruchi Shah, Riddhi Bhavsar, Jhanvi Shah, Mili Pandya, Bhagyadhan Patel, Sudhir Shah, Heli Shah, Shalin Shah, Shruti Bajaj, Siddharth Shah, Nilam Thaker, Umesh Kalane, Mahesh Kamate, Vykunta Raju KN, Naresh Tayade, Sujatha Jagadeesan, Deepika Jain, Mitesh Chandarana, Jitendra Singh, Sanjiv Mehta, Beena Suresh, Harsh Sheth
المصدر: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-17 (2024)
مصطلحات موضوعية: Rare diseases, Diagnosis, IEM, Neuromuscular, Neurodevelopmental disorders, Lysosomal storage diseases, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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2دورية أكاديمية
المؤلفون: Manqi Liang, Beena Suresh, Eric Bareke, Sanaa Choufani, Sujatha Jagadeesh, Rosanna Weksberg, Jacek Majewski, Rima Slim
المصدر: Molecular Genetics & Genomic Medicine, Vol 12, Iss 2, Pp n/a-n/a (2024)
مصطلحات موضوعية: abnormaliy, failure of Meiosis II, HORMAD2, Meiosis, recurrent miscarriage, triploid digynic, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2324-9269
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3دورية أكاديمية
المؤلفون: Beena Suresh, Umarani Ravichandran, Sujatha Jagadeesh
المصدر: Journal of Clinical and Diagnostic Research, Vol 17, Iss 12, Pp 01-03 (2023)
مصطلحات موضوعية: anaemia, heterozygous carrier, molecular testing, prenatal testing, Medicine
وصف الملف: electronic resource
Relation: https://www.jcdr.net/articles/PDF/18819/67494_CE[Ra1]_F(SL)_QC(KK_RDW_SHU)_PF1(VD_KM_OM)_PFA(VD_KM)_PN(KM).pdf; https://doaj.org/toc/2249-782X; https://doaj.org/toc/0973-709X
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4دورية أكاديمية
المؤلفون: Reetika Malik Yadav, Maya Gupta, Aparna Dalvi, Umair Ahmed Bargir, Gouri Hule, Snehal Shabrish, Jahnavi Aluri, Manasi Kulkarni, Priyanka Kambli, Ramya Uppuluri, Suresh Seshadri, Sujatha Jagadeesh, Beena Suresh, Jayarekha Raja, Prasad Taur, Sivasankar Malaischamy, Priyanka Ghosh, Shweta Mahalingam, Priya Kadam, Harsha Prasada Lashkari, Parag Tamhankar, Vasundhara Tamhankar, Shilpa Mithbawkar, Sagar Bhattad, Prerna Jhawar, Adinarayan Makam, Vandana Bansal, Malathi Prasad, Geeta Govindaraj, Beena Guhan, Karthik Bharadwaj Tallapaka, Mukesh Desai, Revathi Raj, Manisha Rajan Madkaikar
المصدر: Frontiers in Immunology, Vol 11 (2020)
مصطلحات موضوعية: prenatal diagnosis, chorionic villus sampling, maternal contamination, cordocentesis, flow cytometry, variants of unknown significance, Immunologic diseases. Allergy, RC581-607
وصف الملف: electronic resource
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5
المؤلفون: Maryam Rezaei, Beena Suresh, Eric Bereke, Zahra Hadipour, Monic Aguinaga, Jianhua Qian, Rashmi Bagga, Majid Fardaei, Reda Hemida, Sujatha Jagadeesh, Jacek Majewski, Rima Slim
المصدر: Clinical Genetics. 99
مصطلحات موضوعية: Genetics, Genetics (clinical)
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6
المؤلفون: Maryam, Rezaei, Beena, Suresh, Eric, Bereke, Zahra, Hadipour, Monica, Aguinaga, Jianhua, Qian, Rashmi, Bagga, Majid, Fardaei, Reda, Hemida, Sujatha, Jagadeesh, Jacek, Majewski, Rima, Slim
المصدر: Clinical geneticsREFERENCES. 99(6)
مصطلحات موضوعية: Beckwith-Wiedemann Syndrome, Placenta, Nuclear Proteins, Hydatidiform Mole, Autoantigens, Mitochondrial Proteins, Protein-Arginine Deiminase Type 6, Pregnancy, Mutation, Uterine Neoplasms, Oocytes, Humans, Female, Neoplasm Recurrence, Local, Adaptor Proteins, Signal Transducing
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7
المؤلفون: Rashmi, Dongerdiye, Sujatha, Jagadeesh, Beena, Suresh, Aruna, Rajendran, Rati, Devendra, Prashant, Warang, Prabhakar S, Kedar
المصدر: Journal of clinical pathology. 74(10)
مصطلحات موضوعية: Adult, Male, Anemia, Hemolytic, Heredity, Developmental Disabilities, DNA Mutational Analysis, Homozygote, Age Factors, Mutation, Missense, High-Throughput Nucleotide Sequencing, India, Severity of Illness Index, Pedigree, Young Adult, Child Development, Phenotype, Child, Preschool, Hexokinase, Exome Sequencing, Humans, Female, Genetic Predisposition to Disease
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8دورية أكاديمية
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9
المؤلفون: Sujatha, Jagadeesh, Beena, Suresh, Suresh, Seshadri, Yoichi, Suzuki
المصدر: The National medical journal of India. 26(1)
مصطلحات موضوعية: Biotinidase Deficiency, Fatal Outcome, Seizures, Infant, Newborn, Humans, Ichthyosis, Alopecia, Female
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::8ccccca22e222424466388946a9ada83
https://pubmed.ncbi.nlm.nih.gov/24066991