Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Kristen Holland
Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14
American Journal of Human Genetics
Genetics
Related publications
Dermatopathia Pigmentosa Reticularis With Salzmann’s Nodular Degeneration of Cornea: A Rare Association
Nepalese journal of ophthalmology : a biannual peer-reviewed academic journal of the Nepal Ophthalmic Society : NEPJOPH
Medicine
A New Case of Keratin 14 Functional Knockout Causes Severe Recessive EBS and Questions the Haploinsufficiency Model of Naegeli–Franceschetti–Jadassohn Syndrome
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Dermatopathia Pigmentosa Reticularis: A Report of a Case With Delayed Onset Alopecia and Onychodystrophy
JAAD Case Reports
Dermatology
Ectodermal Dysplasias Revisited
Acta geneticae medicae et gemellologiae
220 Two Cases of Hypohidrotic Ectodermal Dysplasia Caused by Novel Mutations in the EDA Gene
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
DLX Genes, P63, and Ectodermal Dysplasias
Birth Defects Research Part C - Embryo Today: Reviews
Medicine
Embryology
Developmental Biology
Ectodermal Dysplasias: Classification and Organization by Phenotype, Genotype and Molecular Pathway
American Journal of Medical Genetics, Part A
Genetics
Phenotype-Genotype Correlations in Autosomal Dominant Retinitis Pigmentosa Caused by RHO, D190N
Current Eye Research
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Crisponi Syndrome Is Caused by Mutations in the CRLF1 Gene and Is Allelic to Cold-Induced Sweating Syndrome Type 1
American Journal of Human Genetics
Genetics
