Lawrence Layman
3PUBLICATIONS
39CO-AUTHORS
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Publications (3)
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|Apr 14, 2025
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 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
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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
