Overview
Frederique Bena-Sloan practices practicing medicine in Geneve, Switzerland.
Ms. Bena-Sloan is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Chromosome 6 Uniparental Disomy, Paris-Trousseau Thrombocytopenia, Jacobsen Syndrome, and Mosaic Trisomy 8.
She is actively involved in clinical research, co-authoring 28 peer reviewed articles.
Gender
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Frequently Asked Questions about Frederique Bena-Sloan
Is Frederique Bena-Sloan a top-rated expert for Chromosome 6 Uniparental Disomy?
MediFind is an objective health platform that identifies experts based on real-world data. Frederique Bena-Sloan is classified as an Distinguished expert for Chromosome 6 Uniparental Disomy, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Frederique Bena-Sloan participate in research or clinical trials?
Yes. Frederique Bena-Sloan has published 28 articles and abstracts on conditions like Chromosome 6 Uniparental Disomy. You can view a list of Frederique Bena-Sloan's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Distinguished
- Chromosome 6 Uniparental DisomyMs. Bena-Sloan isDistinguished. Learn about Chromosome 6 Uniparental Disomy.
- Experienced
- Arthrogryposis Multiplex CongenitaMs. Bena-Sloan isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Chromosome 8p DeletionMs. Bena-Sloan isExperienced. Learn about Chromosome 8p Deletion.
- Chronic Granulomatous DiseaseMs. Bena-Sloan isExperienced. Learn about Chronic Granulomatous Disease.
- Congenital AfibrinogenemiaMs. Bena-Sloan isExperienced. Learn about Congenital Afibrinogenemia.
- Congenital ContracturesMs. Bena-Sloan isExperienced. Learn about Congenital Contractures.
- DiGeorge SyndromeMs. Bena-Sloan isExperienced. Learn about DiGeorge Syndrome.
- Down SyndromeMs. Bena-Sloan isExperienced. Learn about Down Syndrome.
- Familial HypofibrinogenemiaMs. Bena-Sloan isExperienced. Learn about Familial Hypofibrinogenemia.
- Gestational Trophoblastic DiseaseMs. Bena-Sloan isExperienced. Learn about Gestational Trophoblastic Disease.
- Hydatidiform MoleMs. Bena-Sloan isExperienced. Learn about Hydatidiform Mole.
- HypoparathyroidismMs. Bena-Sloan isExperienced. Learn about Hypoparathyroidism.
- Immune Defect due to Absence of ThymusMs. Bena-Sloan isExperienced. Learn about Immune Defect due to Absence of Thymus.
- IntersexMs. Bena-Sloan isExperienced. Learn about Intersex.
- Jacobsen SyndromeMs. Bena-Sloan isExperienced. Learn about Jacobsen Syndrome.
- Mosaic Trisomy 8Ms. Bena-Sloan isExperienced. Learn about Mosaic Trisomy 8.
- MosaicismMs. Bena-Sloan isExperienced. Learn about Mosaicism.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Paris-Trousseau ThrombocytopeniaMs. Bena-Sloan isExperienced. Learn about Paris-Trousseau Thrombocytopenia.
- Turner SyndromeMs. Bena-Sloan isExperienced. Learn about Turner Syndrome.