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Lawrence Layman

3PUBLICATIONS
39CO-AUTHORS
Polymerisation mechanismsNeurogenetics
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Journal

Publications (3)

Sort by Publication Date:
|Apr 14, 2025
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of <i>PGAP2</i> Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3).

Seda Susgun, Afif Ben-Mahmoud, Franz Rüschendorf

|Jul 11, 2022
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function.

Sheng-Jia Lin, Barbara Vona, Hillary M Porter

|Aug 18, 2021
Twenty-year follow-up of the facial phenotype of Brazilian patients with Sotos syndrome.

Matheus Augusto Araújo Castro, Juliana Heather Vedovato Dos Santos, Rachel Sayuri Honjo

Pageof 1

Frequent Collaborators

3 joint publications

Hyung-Goo Kim

2 joint publications

Yves Lacassie

2 joint publications

Lynn P Chorich

2 joint publications

Saadullah Khan

2 joint publications

Franz Rüschendorf

1 joint publications

Gaurav K Varshney

1 joint publications

Juliana Heather Vedovato Dos Santos

1 joint publications

Rachel Sayuri Honjo

1 joint publications

Débora Romeo Bertola

1 joint publications

Anna C Hurst

Frequent Collaborators

3 joint publications

Hyung-Goo Kim

2 joint publications

Yves Lacassie

2 joint publications

Lynn P Chorich

2 joint publications

Saadullah Khan

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