Jwalant E. Waghmare

Wardha, MH, India

Last Updated: 09/26/2026

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Found 13 publications

Association of GATA4 Gene Variants with Congenital Heart Disease: A Case-control Study.

Association of GATA4 Gene Variants with Congenital Heart Disease: A Case-control Study.

Journal: Annals of African medicine
Published: April 27, 2026

Assessment of Knowledge, Awareness, and Attitude toward Premarital Screening for Sickle Cell Disease among Young Adults in Central India - A Cross-sectional Study.

Assessment of Knowledge, Awareness, and Attitude toward Premarital Screening for Sickle Cell Disease among Young Adults in Central India - A Cross-sectional Study.

Journal: Annals of African medicine
Published: December 26, 2025

Rare 48, XXYY Syndrome with Primary Infertility and Behavioural Disorder: A Case Report.

Rare 48, XXYY Syndrome with Primary Infertility and Behavioural Disorder: A Case Report.

Journal: Journal of human reproductive sciences
Published: February 27, 2025

Molecular characterization of de novo ring chromosome 21 in a child with seizures, growth retardation, and multiple congenital anomalies.

Molecular characterization of de novo ring chromosome 21 in a child with seizures, growth retardation, and multiple congenital anomalies.

Journal: Journal of genetics
Published: September 21, 2023

Assessment of Oxidative Stress Biomarkers and Body Mass Index in Pulmonary Tuberculosis Patients: A Case-Control Study.

Assessment of Oxidative Stress Biomarkers and Body Mass Index in Pulmonary Tuberculosis Patients: A Case-Control Study.

Journal: Nigerian medical journal : journal of the Nigeria Medical Association
Published: April 26, 2022

The association of testis-specific hTAF7L gene variants with idiopathic azoospermic and severe oligozoospermic male infertility.

The association of testis-specific hTAF7L gene variants with idiopathic azoospermic and severe oligozoospermic male infertility.

Journal: Andrologia
Published: January 13, 2022

A missense mutation (c.226C>A) in HMG box SRY gene affects nNLS function in 46,XY sex reversal female.

A missense mutation (c.226C>A) in HMG box SRY gene affects nNLS function in 46,XY sex reversal female.

Journal: Andrologia
Published: December 15, 2020

Chromosomal Aberrations in Couples with Pregnancy Loss: A Retrospective Study.

Chromosomal Aberrations in Couples with Pregnancy Loss: A Retrospective Study.

Journal: Journal of human reproductive sciences
Published: December 21, 2018

Computed Tomographic Estimation of Relationship between Renal Volume and Body Weight of an Individual.

Computed Tomographic Estimation of Relationship between Renal Volume and Body Weight of an Individual.

Journal: Journal of clinical and diagnostic research : JCDR
Published: November 08, 2016

Large Scale 7436-bp Deletions in Human Sperm Mitochondrial DNA with Spermatozoa Dysfunction and Male Infertility.

Large Scale 7436-bp Deletions in Human Sperm Mitochondrial DNA with Spermatozoa Dysfunction and Male Infertility.

Journal: Journal of clinical and diagnostic research : JCDR
Published: June 29, 2016

Prevalence of Y Chromosome Microdeletions in Idiopathic Azoospermia Cases in Central Indian Men.

Prevalence of Y Chromosome Microdeletions in Idiopathic Azoospermia Cases in Central Indian Men.

Journal: Journal of clinical and diagnostic research : JCDR
Published: June 17, 2015

Dermatoglyphics and karyotype analysis in primary amenorrhoea.

Dermatoglyphics and karyotype analysis in primary amenorrhoea.

Journal: Journal of clinical and diagnostic research : JCDR
Published: June 12, 2014
Showing 1-12 of 13

Last Updated: 09/26/2026