Harold E Cross

3PUBLICATIONS
21CO-AUTHORS
Gene mappingHaematological tumours
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Publications (3)

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|Sep 27, 2021
A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder.

Zineb Ammous, Lettie E Rawlins, Hannah Jones

|Nov 20, 2020
No association between SCN9A and monogenic human epilepsy disorders.

James Fasham, Joseph S Leslie, Jamie W Harrison

|Jan 13, 2017
Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice.

Martina M A Muggenthaler, Biswajit Chowdhury, S Naimul Hasan

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Frequent Collaborators

2 joint publications

Barry A Chioza

2 joint publications

Joseph S Leslie

2 joint publications

Emma L Baple

1 joint publications

Biswajit Chowdhury

1 joint publications

Elijah R Behr

1 joint publications

Kenneth Zahka

1 joint publications

Fowzan S Alkuraya

1 joint publications

Barbara Triggs-Raine

1 joint publications

James Fasham

1 joint publications

Jamie W Harrison

Frequent Collaborators

2 joint publications

Barry A Chioza

2 joint publications

Joseph S Leslie

2 joint publications

Emma L Baple

1 joint publications

Biswajit Chowdhury

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