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Co-Occurrence of Leber Congenital Amaurosis and Meckel Syndrome Type 1 in a Fetus: Is There a Lesson to Be Learned
Author(s) -
Karthik Bharadwaj Tallapaka,
Shagun Aggarwal,
Amrita Bhattacherjee,
Aneek Das Bhowmik,
Ashwin Dalal
Publication year - 2019
Publication title -
molecular syndromology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.609
H-Index - 36
eISSN - 1661-8777
pISSN - 1661-8769
DOI - 10.1159/000496280
Subject(s) - fetus , medicine , pregnancy , sibling , pediatrics , exome sequencing , mutation , gene , genetics , biology , psychology , developmental psychology

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