Sapna Sandal
New Delhi, DL, India
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Next-Generation Sequencing in Unexplained Intellectual Disability.
Journal: Indian journal of pediatrics
Published: December 11, 2022
Progress in Diagnosis and Management of Intellectual Disability in India: A Journey Over Half-a-Century!
Journal: Indian pediatrics
Published: November 12, 2022
Desmin Myopathy-A Masquerader of Infantile-Onset Pompe Disease.
Journal: Indian journal of pediatrics
Published: May 08, 2022
Clinico-radiological and biochemical clues to early diagnosis of mucolipidosis type II.
Journal: Clinical dysmorphology
Published: September 25, 2021
Prenatal phenotypic spectrum of full trisomy 18 in an Indian cohort.
Journal: American journal of medical genetics. Part A
Published: December 26, 2020
Alpha-mannosidosis in a family: natural history with an uncommon retinal dystrophy.
Journal: Clinical dysmorphology
Published: December 08, 2020
ANO5-associated Gnathodiaphyseal dysplasia with calvarial doughnut lesions: First report in an Asian Indian with an expanded phenotype.
Journal: Congenital anomalies
Published: June 09, 2020
Hypophosphatemic Rickets with R179W Mutation in FGFR23 Gene - A Rare But Treatable Cause of Refractory Rickets.
Journal: Indian journal of pediatrics
Published: March 20, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026