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Article

KBG syndrome: 16q24.3 microdeletion in an Indian patient.

Clinical dysmorphology - 1 Jul 2017

Srivastava Priyanka, Gambhir Poonam S, Phadke Shubha R

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Identifiers

PMID: 28099180
DOI: 10.1097/MCD.0000000000000168

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 9 Sept 2026.

Related research

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KBG syndrome: 16q24.3 microdeletion in an Indian patient.PMID 28099180Read ↗

A case of prenatal diagnosis of 16q24.3 microdeletion KBG syndrome and review of the literatureSemantic proximity Read ↗

KBG Syndrome in 16 Indian Individuals.Semantic proximity Read ↗

A Chinese patient with KBG syndrome and a 9q31.2-33.1 microdeletion.Semantic proximity Read ↗

Partial deletion of ANKRD11 results in the KBG phenotype distinct from the 16q24.3 microdeletion syndrome.Semantic proximity Read ↗

Phenotypes of 8q13.2-q13.3 microdeletion: Case report and literature review of an emerging recurrent microdeletion syndrome.Semantic proximity Read ↗

Mayer–Rokitansky–Küster–Hauser Syndrome and 16p11.2 Recurrent Microdeletion: A Case Report and Review of the LiteratureSemantic proximity Read ↗

Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11.Semantic proximity Read ↗

A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion.Semantic proximity Read ↗

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