Samin A Sajan

2PUBLICATIONS
0CO-AUTHORS
Infant and child healthGene expression (incl. microarray and other genome-wide approaches)
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Publications (2)

|Nov 28, 2018
Biallelic disruption of PKDCC is associated with a skeletal disorder characterised by rhizomelic shortening of extremities and dysmorphic features.

Samin A Sajan, Jaya Ganesh, Deepali N Shinde

|Jul 11, 2018
Diagnostic exome sequencing identifies GLI2 haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomalies.

Samin A Sajan, Zöe Powis, Katherine L Helbig

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