Laura K Conlin

4PUBLICATIONS
31CO-AUTHORS
Cell and nuclear divisionGenetic immunologyInformation systems development methodologies and practiceFoetal development and medicine
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Publications (4)

|Oct 25, 2026
Overcoming a diagnostic blindspot: Identifying balanced translocations in Mendelian rare disease cohorts.

|Jun 01, 2019
Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and management.

Sarah E Sheppard, Emilie Lalonde, N Scott Adzick

|Nov 05, 2016
A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.

Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola

|Aug 07, 2015
Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure.

Surabhi Mulchandani, Elizabeth J Bhoj, Minjie Luo

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Frequent Collaborators

1 joint publications

Tejas Jammihal

1 joint publications

Cecelia Esteves

1 joint publications

Shilpa Nadimpalli Kobren

1 joint publications

Ramakrishnan Rajagopalan