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Shalini S Nayak

Showing results (1-10 of 38) with videos related to

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Indian Pediatrics|February 2, 2015
Anomalies associated with single umbilical artery at perinatal autopsyShalini S Nayak, Anju Shukla, Katta M Girisha
Clinical Dysmorphology|December 1, 2023
Comprehensive phenotyping of fetuses with trisomy 18: a perinatal center experienceMangalore S Shravya, Katta M Girisha, Shalini S Nayak
Clinical Neurology and Neurosurgery|January 4, 2025
A microanatomical study of the precentral cerebral wall in human fetuses of the second trimester with ventriculomegaly and corpus callosal dysgenesisVeeresh, Shalini S Nayak, Deepak Nayak, et al.
Congenital Anomalies|December 15, 2015
Spectrum of urorectal septum malformation sequenceKrupa Shah, Shalini S Nayak, Anju Shukla, et al.
American Journal of Medical Genetics. Part A|December 28, 2019
Biallelic c.1263dupC in DOK7 results in fetal akinesia deformation sequencePeriyasamy Radhakrishnan, Anju Shukla, Katta M Girisha, et al.
Clinical Dysmorphology|July 10, 2018
Facial profile and additional features in fetuses with trisomy 21Periyasamy Radhakrishnan, Shalini S Nayak, Anju Shukla, et al.
Clinical Dysmorphology|January 14, 2025
Biallelic variants in AGRN with recurrent pregnancy losses in a family with a fetal akinesia deformation sequenceMangalore S Shravya, Ankur Chaurasia, Katta M Girisha, et al.
Journal of Clinical and Diagnostic Research : JCDR|October 27, 2015
Middle Interhemispheric Variant of Holoprosencephaly - Presenting as Non-Visualized Cavum Septum Pellucidum and An Interhemispheric Cyst in A 19-Weeks FetusAkhila Vasudeva, Shalini S Nayak, Rajagopal Kadavigere, et al.
Congenital Anomalies|September 15, 2016
Variable presentation of Fraser syndrome in two fetuses and a novel mutation in FRAS1Shalini S Nayak, Smrithi Salian, Anju Shukla, et al.
Clinical Genetics|August 15, 2019
Meckel syndrome: Clinical and mutation profile in six fetusesPeriyasamy Radhakrishnan, Shalini S Nayak, Anju Shukla, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Indian Pediatrics|February 2, 2015
Anomalies associated with single umbilical artery at perinatal autopsyShalini S Nayak, Anju Shukla, Katta M Girisha
Clinical Dysmorphology|December 1, 2023
Comprehensive phenotyping of fetuses with trisomy 18: a perinatal center experienceMangalore S Shravya, Katta M Girisha, Shalini S Nayak
Clinical Neurology and Neurosurgery|January 4, 2025
A microanatomical study of the precentral cerebral wall in human fetuses of the second trimester with ventriculomegaly and corpus callosal dysgenesisVeeresh, Shalini S Nayak, Deepak Nayak, et al.
Congenital Anomalies|December 15, 2015
Spectrum of urorectal septum malformation sequenceKrupa Shah, Shalini S Nayak, Anju Shukla, et al.
American Journal of Medical Genetics. Part A|December 28, 2019
Biallelic c.1263dupC in DOK7 results in fetal akinesia deformation sequencePeriyasamy Radhakrishnan, Anju Shukla, Katta M Girisha, et al.
Clinical Dysmorphology|July 10, 2018
Facial profile and additional features in fetuses with trisomy 21Periyasamy Radhakrishnan, Shalini S Nayak, Anju Shukla, et al.
Clinical Dysmorphology|January 14, 2025
Biallelic variants in AGRN with recurrent pregnancy losses in a family with a fetal akinesia deformation sequenceMangalore S Shravya, Ankur Chaurasia, Katta M Girisha, et al.
Journal of Clinical and Diagnostic Research : JCDR|October 27, 2015
Middle Interhemispheric Variant of Holoprosencephaly - Presenting as Non-Visualized Cavum Septum Pellucidum and An Interhemispheric Cyst in A 19-Weeks FetusAkhila Vasudeva, Shalini S Nayak, Rajagopal Kadavigere, et al.
Congenital Anomalies|September 15, 2016
Variable presentation of Fraser syndrome in two fetuses and a novel mutation in FRAS1Shalini S Nayak, Smrithi Salian, Anju Shukla, et al.
Clinical Genetics|August 15, 2019
Meckel syndrome: Clinical and mutation profile in six fetusesPeriyasamy Radhakrishnan, Shalini S Nayak, Anju Shukla, et al.
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