Jagadeesh Sujatha: search on Z-Library

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1

Locus and allelic heterogeneity and phenotypic variability in Waardenburg syndrome

Somashekar, Puneeth H., Girisha, Katta M., Nampoothiri, Sheela, Gowrishankar, Kalpana, Rama Devi, Radha, Gupta, Neerja, Narayanan, Dhanya Lakshmi, Kaur, Anupriya, Bajaj, Shruti, Jagadeesh, Sujatha, Le

Journal:

Clinical Genetics

Year:

2018

Language:

english

File:

PDF, 1.12 MB

english, 2018

2

Down’s Syndrome Screening in the First Trimester with Additional Serum Markers: Indian Parameters

Suresh, Seshandri, Cuckle, Howard S., Jagadeesh, Sujatha, Ghosh, Kushagradhi, Vemavarapu, Gayathri, Taval, Tulika, Suresh, Sudarshan

Journal:

The Journal of Obstetrics and Gynecology of India

Year:

2019

Language:

english

File:

PDF, 578 KB

english, 2019

3

Second trimester diagnosis of Neu Laxova syndrome

M. A. Shivarajan, S. Suresh, Sujatha Jagadeesh, S. Lata, Lathaa Bhat

Journal:

Prenatal Diagnosis

Year:

2003

Language:

english

File:

PDF, 123 KB

english, 2003

4

Triple X syndrome with rare phenotypic presentation

Sujatha Jagadeesh, Gazala Jabeen, Lathaa Bhat, Madhavi Vasikarla, Arvind Suresh, Suresh Seshadri, S. Lata

Journal:

Indian Journal of Pediatrics

Year:

2008

Language:

english

File:

PDF, 806 KB

english, 2008

5

Perinatal outcome after multifetal pregnancy reduction

Seshadri Suresh, Suresh Indrani, Gurusamy Thangavel, Jagadeesh Sujatha

Journal:

Indian Journal of Pediatrics

Year:

2008

Language:

english

File:

PDF, 150 KB

english, 2008

6

Fanconi–Bickel Syndrome

Mohandas Nair K, Osamu Sakamoto, Sujatha Jagadeesh, Sheela Nampoothiri

Journal:

Indian Journal of Pediatrics

Year:

2012

Language:

english

File:

PDF, 131 KB

english, 2012

7

Cartilage-hair hypoplasia caused by novel compound heterozygousRMRPmutations

Kerstin Reicherter, Amithkumar Iynapillai Veeramani, Sujatha Jagadeesh

Journal:

Indian Pediatrics

Year:

2011

Language:

english

File:

PDF, 180 KB

english, 2011

8

Citrullinemia type 1: Genetic diagnosis and prenatal diagnosis in subsequent pregnancy

Karthikeyan, G., Jagadeesh, Sujatha, Seshadri, Suresh, Häberle, J.

Journal:

Indian Pediatrics

Year:

2013

Language:

english

File:

PDF, 390 KB

english, 2013

9

Clinical and biochemical features guiding the diagnostics in neurometabolic cutis laxa

Gardeitchik, Thatjana, Mohamed, Miski, Fischer, Björn, Lammens, Martin, Lefeber, Dirk, Lace, Baiba, Parker, Michael, Kim, Ki-Joong, Lim, Bing C, Häberle, Johannes, Garavelli, Livia, Jagadeesh, Sujatha

Journal:

European Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.22 MB

english, 2014

10

Genetic counseling in chromosomal abnormalities

Bansal, Vandana, Suresh, S, Suresh, Indrani, Jagadeesh, Sujatha, Fazal, GazalaJabeen

Journal:

Journal of Prenatal Diagnosis and Therapy

Year:

2010

Language:

english

File:

PDF, 1.62 MB

english, 2010

11

Pyridoxine-dependent epilepsy owing to antiquitin deficiency — mutation in the ALDH7A1 gene

Jagadeesh, Sujatha, Suresh, Beena, Murugan, V, Suresh, S, Salomans, G S, Struys, E A, Jacobs, C

Journal:

Paediatrics and International Child Health

Year:

2013

Language:

english

File:

PDF, 81 KB

english, 2013

12

Normative data for stretched penile length in term neonates born in Tamil Nadu

Prabhu, SudhaRathna, Mahadevan, Shriraam, Bharath, R, Jagadeesh, Sujatha, Kumutha, J, Suresh, Seshadri

Journal:

Indian Journal of Endocrinology and Metabolism

Year:

2014

Language:

english

File:

PDF, 621 KB

english, 2014

13

Congenital Hypothyroidism: Recent Indian data

Mahadevan, Shriraam, Jagadeesh, Sujatha, Suresh, Seshadri, Prabhu, SudhaRathna

Journal:

Indian Journal of Endocrinology and Metabolism

Year:

2015

Language:

english

File:

PDF, 325 KB

english, 2015

14

Mutations in ARSB in MPS VI patients in India

Mathew, Juby, Jagadeesh, Sujatha M., Bhat, Meenakshi, Udhaya Kumar, S., Thiyagarajan, Saravanamuthu, Srinivasan, Sudha

Journal:

Molecular Genetics and Metabolism Reports

Year:

2015

Language:

english

File:

PDF, 2.71 MB

english, 2015

15

Usefulness of fetal autopsy in the diagnosis of blomstrand chondrodysplasia: a report of three cases

Beena, Suresh, Murlidhar, Lata, Seshadri, Suresh, Jagadeesh, Sujatha, Suresh, Indrani

Journal:

Journal of Maternal-Fetal and Neonatal Medicine

Year:

2016

Language:

english

File:

PDF, 895 KB

english, 2016

16

Additional three patients with Smith-McCort dysplasia due to novel RAB33B mutations

Salian, Smrithi, Cho, Tae-Joon, Phadke, Shubha R., Gowrishankar, Kalpana, Bhavani, Gandham SriLakshmi, Shukla, Anju, Jagadeesh, Sujatha, Kim, Ok-Hwa, Nishimura, Gen, Girisha, Katta M.

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 1.52 MB

english, 2017

17

Cover Image, Volume 173A, Number 3, March 2017

Salian, Smrithi, Cho, Tae-Joon, Phadke, Shubha R., Gowrishankar, Kalpana, Bhavani, Gandham SriLakshmi, Shukla, Anju, Jagadeesh, Sujatha, Kim, Ok-Hwa, Nishimura, Gen, Girisha, Katta M.

Journal:

American Journal of Medical Genetics Part A

Year:

2017

File:

PDF, 825 KB

2017

18

Persistent Left Superior Vena Cava in Fetuses—An Autopsy Series

Ramakrishnan, Deepa, Chidambarathanu, Shanthi, Murli, Lata, Micheal, John, Jagadeesh, Sujatha, Suresh, Indrani, Seshadri, Suresh

Journal:

Fetal and Pediatric Pathology

Year:

2017

Language:

english

File:

PDF, 703 KB

english, 2017

19

The First Trimester Combined Screening Test in the Indian Population: Insights from a Cohort of 27,647 Pregnancies

Manikandan, K., Rangaraj, Aarthi, Ganesan, Ponmozhi, Reddy, Vaishnavi, Suresh, Sudarshan, Jagadeesh, Sujatha M., Suresh, Indrani, Seshadri, Suresh

Journal:

Journal of Fetal Medicine

Year:

2017

Language:

english

File:

PDF, 571 KB

english, 2017

20

Normative Data of Thyroid Gland Volume in South Indian Neonates and Infants

Prabhu, Sudha Rathna, Mahadevan, Shriraam, Jagadeesh, Sujatha, Dharan, Dharani, Ganesh, Chandra, Suresh, Seshadri, Suresh, Indrani

Journal:

Indian Journal of Pediatrics

Year:

2018

Language:

english

File:

PDF, 362 KB

english, 2018

21

The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients

Nguyen, Ngoc Minh Phuong, Khawajkie, Yassemine, Mechtouf, Nawel, Rezaei, Maryam, Breguet, Magali, Kurvinen, Elvira, Jagadeesh, Sujatha, Solmaz, Asli Ece, Aguinaga, Monica, Hemida, Reda, Harma, Mehmet

Journal:

Modern Pathology

Year:

2018

Language:

english

File:

PDF, 2.41 MB

english, 2018

22

Idiopathic Arterial Calcification: Experience from a Single Center in South India

Colaco, Sylvia M., Chidambarathanu, Shanthi, Raja, Vijayalakshmi, Murlidhar, Lata, Jagadeesh, Sujatha, Suresh, Indrani, Seshadri, Suresh

Journal:

Journal of Fetal Medicine

Year:

2018

Language:

english

File:

PDF, 659 KB

english, 2018

23

Ptosis as a unique hallmark for autosomal recessive WNT1 ‐associated osteogenesis imperfecta

Nampoothiri, Sheela, Guillemyn, Brecht, Elcioglu, Nursel, Jagadeesh, Sujatha, Yesodharan, Dhanya, Suresh, Beena, Turan, Serap, Symoens, Sofie, Malfait, Fransiska

Journal:

American Journal of Medical Genetics Part A

Year:

2019

Language:

english

File:

PDF, 1.24 MB

english, 2019

24

A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV)

Suresh, Beena, Reddy, Vaishnavi, Kurth, Ingo, Jagadeesh, Sujatha

Journal:

Neuro-Ophthalmology

Year:

2018

Language:

english

File:

PDF, 580 KB

english, 2018

25

A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV)

Suresh, Beena, Reddy, Vaishnavi, Kurth, Ingo, Jagadeesh, Sujatha

Journal:

Neuro-Ophthalmology

Year:

2018

File:

PDF, 580 KB

2018

26

Bain type of X‐linked syndromic mental retardation in a male with a pathogenic variant in HNRNPH2

Somashekar, Puneeth H., Narayanan, Dhanya L., Jagadeesh, Sujatha, Suresh, Beena, Vaishnavi, Reddy D., Bielas, Stephanie, Girisha, Katta M., Shukla, Anju

Journal:

American Journal of Medical Genetics Part A

Year:

2019

Language:

english

File:

PDF, 1.19 MB

english, 2019

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