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Sujatha Jagadeesh

Showing results (11-20 of 38) with videos related to

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Indian Journal of Endocrinology and Metabolism|August 22, 2014
Normative data for stretched penile length in term neonates born in Tamil NaduSudha Rathna Prabhu, Shriraam Mahadevan, R Bharath, et al.
Indian Journal of Pediatrics|September 2, 2008
Triple X syndrome with rare phenotypic presentationSujatha Jagadeesh, Gazala Jabeen, Lathaa Bhat, et al.
Fetal and Pediatric Pathology|June 2, 2017
Persistent Left Superior Vena Cava in Fetuses: An Autopsy SeriesDeepa Ramakrishnan, Shanthi Chidambarathanu, Lata Murli, et al.
Journal of Obstetrics and Gynaecology of India|February 8, 2020
Down's Syndrome Screening in the First Trimester with Additional Serum Markers: Indian ParametersSeshandri Suresh, Howard S Cuckle, Sujatha Jagadeesh, et al.
Journal of Clinical Pathology|December 28, 2020
Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the <i>HK1</i> gene causing severe haemolytic anaemia with developmental delay in an Indian familyRashmi Dongerdiye, Sujatha Jagadeesh, Beena Suresh, et al.
Indian Journal of Pediatrics|February 10, 2018
Normative Data of Thyroid Gland Volume in South Indian Neonates and InfantsSudha Rathna Prabhu, Shriraam Mahadevan, Sujatha Jagadeesh, et al.
Molecular Genetics & Genomic Medicine|February 24, 2024
A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriageManqi Liang, Beena Suresh, Eric Bareke, et al.
Paediatrics and International Child Health|August 9, 2013
Pyridoxine-dependent epilepsy owing to antiquitin deficiency--mutation in the ALDH7A1 geneSujatha Jagadeesh, Beena Suresh, V Murugan, et al.
American Journal of Medical Genetics. Part A|March 22, 2019
Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfectaSheela Nampoothiri, Brecht Guillemyn, Nursel Elcioglu, et al.
American Journal of Medical Genetics. Part A|November 1, 2019
Bain type of X-linked syndromic mental retardation in a male with a pathogenic variant in HNRNPH2Puneeth H Somashekar, Dhanya L Narayanan, Sujatha Jagadeesh, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Indian Journal of Endocrinology and Metabolism|August 22, 2014
Normative data for stretched penile length in term neonates born in Tamil NaduSudha Rathna Prabhu, Shriraam Mahadevan, R Bharath, et al.
Indian Journal of Pediatrics|September 2, 2008
Triple X syndrome with rare phenotypic presentationSujatha Jagadeesh, Gazala Jabeen, Lathaa Bhat, et al.
Fetal and Pediatric Pathology|June 2, 2017
Persistent Left Superior Vena Cava in Fetuses: An Autopsy SeriesDeepa Ramakrishnan, Shanthi Chidambarathanu, Lata Murli, et al.
Journal of Obstetrics and Gynaecology of India|February 8, 2020
Down's Syndrome Screening in the First Trimester with Additional Serum Markers: Indian ParametersSeshandri Suresh, Howard S Cuckle, Sujatha Jagadeesh, et al.
Journal of Clinical Pathology|December 28, 2020
Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the <i>HK1</i> gene causing severe haemolytic anaemia with developmental delay in an Indian familyRashmi Dongerdiye, Sujatha Jagadeesh, Beena Suresh, et al.
Indian Journal of Pediatrics|February 10, 2018
Normative Data of Thyroid Gland Volume in South Indian Neonates and InfantsSudha Rathna Prabhu, Shriraam Mahadevan, Sujatha Jagadeesh, et al.
Molecular Genetics & Genomic Medicine|February 24, 2024
A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriageManqi Liang, Beena Suresh, Eric Bareke, et al.
Paediatrics and International Child Health|August 9, 2013
Pyridoxine-dependent epilepsy owing to antiquitin deficiency--mutation in the ALDH7A1 geneSujatha Jagadeesh, Beena Suresh, V Murugan, et al.
American Journal of Medical Genetics. Part A|March 22, 2019
Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfectaSheela Nampoothiri, Brecht Guillemyn, Nursel Elcioglu, et al.
American Journal of Medical Genetics. Part A|November 1, 2019
Bain type of X-linked syndromic mental retardation in a male with a pathogenic variant in HNRNPH2Puneeth H Somashekar, Dhanya L Narayanan, Sujatha Jagadeesh, et al.
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