Robert J. Gorlin and the Dysmorphology Conferences
In Memoriam: Robert J. Gorlin, 1923–2006
Robert J. Gorlin (1923–2006): Teacher, Colleague, and Friend
Robert J. Gorlin, 1923–2006: A Remembrance
Looking Different: Understanding Diversity in Facial Form
The Genetic Basis of Tooth Development and Dental Defects
Molecular Basis of Human Dentin Diseases
The Molecular Etiologies and Associated Phenotypes of Amelogenesis Imperfecta
Craniofacial and Dental Phenotype of Smith–Magenis Syndrome
PVRL1 Variants Contribute to Non-Syndromic Cleft Lip and Palate in Multiple Populations
GLI2 Mutations in Four Brazilian Patients: How Wide Is the Phenotypic Spectrum?
SIX3 Mutations With Holoprosencephaly
PTCH Mutations in Four Brazilian Patients With Holoprosencephaly and in One With Holoprosencephaly-Like Features and Normal MRI
Holoprosencephaly-Like Phenotype: Clinical and Genetic Perspectives
Single Maxillary Central Incisor, Holoprosencephaly, and Holoprosencephaly-Like Phenotype
Contiguous Gene Syndrome of Holoprosencephaly and Hypotrichosis Simplex: Association With an 18p11.3 Deletion
Hutchinson–Gilford Progeria Syndrome: Review of the Phenotype
Patched Mutations and Hairy Skin Patches: A New Sign in Gorlin Syndrome
Clinical Dividends From the Molecular Genetic Diagnosis of Craniosynostosis
A Newly Recognized Polyosteolysis/Hyperostosis Syndrome
The New Bone Biology: Pathologic, Molecular, and Clinical Correlates