Fraser Syndrome Latest Advances

Journal: Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia

Published: February 21, 2023

Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas.

Journal: Diagnostics (Basel, Switzerland)

Published: February 13, 2023

FREM2-related Fraser syndrome with popliteal pterygium and structural central nervous system anomalies.

Journal: European journal of medical genetics

Published: September 16, 2022

"Hypothesis: Patient with possible disturbance in programmed cell death": further insights in pathogenicity and clinical features of Fraser syndrome.

Journal: European journal of human genetics : EJHG

Published: July 07, 2022

Clinical features and orbital anomalies in Fraser syndrome and a review of management options.

Journal: Indian journal of ophthalmology

Published: July 06, 2022

Comprehensive analysis of FRAS1/FREM family as potential biomarkers and therapeutic targets in renal clear cell carcinoma.

Journal: Frontiers in pharmacology

Published: June 19, 2022

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Frem2 Knockout Mice Exhibit Fraser Syndrome Phenotypes and Neonatal Lethality Due to Bilateral Renal Agenesis.

Frem2 Knockout Mice Exhibit Fraser Syndrome Phenotypes and Neonatal Lethality Due to Bilateral Renal Agenesis.

Fraser syndrome with limb reduction defect: a rare and unique anatomic variation.

Fraser syndrome with limb reduction defect: a rare and unique anatomic variation.

The Fraser complex interconnects tissue layers to support basal epidermis and osteoblast integrated morphogenesis underlying fin skeletal patterning.

The Fraser complex interconnects tissue layers to support basal epidermis and osteoblast integrated morphogenesis underlying fin skeletal patterning.

Bilateral cryptophthalmos with overlapping features of Manitoba oculo-tricho-anal (MOTA) syndrome and Fraser syndrome 2.

Bilateral cryptophthalmos with overlapping features of Manitoba oculo-tricho-anal (MOTA) syndrome and Fraser syndrome 2.

Oral and Craniofacial Anomalies of Fraser Syndrome:Prosthetic Management.

Oral and Craniofacial Anomalies of Fraser Syndrome:Prosthetic Management.

The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal-Epidermal Junction of Mouse Skin.

The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal-Epidermal Junction of Mouse Skin.

About a case of Fraser syndrome. Autopsy of a 37 weeks gestation fetus with multiple malformations

About a case of Fraser syndrome. Autopsy of a 37 weeks gestation fetus with multiple malformations

Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas.

Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas.

FREM2-related Fraser syndrome with popliteal pterygium and structural central nervous system anomalies.

FREM2-related Fraser syndrome with popliteal pterygium and structural central nervous system anomalies.

"Hypothesis: Patient with possible disturbance in programmed cell death": further insights in pathogenicity and clinical features of Fraser syndrome.

"Hypothesis: Patient with possible disturbance in programmed cell death": further insights in pathogenicity and clinical features of Fraser syndrome.

Clinical features and orbital anomalies in Fraser syndrome and a review of management options.

Clinical features and orbital anomalies in Fraser syndrome and a review of management options.

Comprehensive analysis of FRAS1/FREM family as potential biomarkers and therapeutic targets in renal clear cell carcinoma.

Comprehensive analysis of FRAS1/FREM family as potential biomarkers and therapeutic targets in renal clear cell carcinoma.