Louise Amlie-Wolf, CGC
GeneticsInsurance Accepted
- Aetna HMO
- Aetna HMO/POS/PPO/EPO
- Aetna PPO/POS/EPO
- Cigna/Great West HMO EPO POS
- Cigna/Great West PPO
- Delaware First Health
- First Health Aetna PPO/EPO
- First Health/Affordable PPO
- Global Medical Managment DE/PA
- Highmark Blue Cross Blue Shield of Delaware
- Highmark Blue Cross Blue Shield of Pennsylvania
- Highmark Medicaid Health Options
- Horizon Blue Cross Blue Shield of New Jersey
- Insurance Administrators of America
- INTEGRA Administrative Group (ClaimsBridge)
- Multiplan PPO
- Plan Vista/NPPN PPO
- Preferred Healthcare PPO
- Private Health Care Systems (PHCS)
- Qualcare HMO/POS/PPO
- Star Healthcare Network
- Three Rivers Provider Network
- Tricare/Humana Military Health Services/CHAMPVA
- United Healthcare of the Mid-Atlantic
- US Family Health Plan
- Volusia Health Network PPO/EPO
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SOX2 pathogenic variants with normal eyes: Expanding the phenotypic spectrum; American Journal of Medical Genetics Part A; (2023).
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Review of 37 patients with SOX2 pathogenic variants collected by the Anophthalmia/Microphthalmia Clinical Registry and DNA research study; American Journal of Medical Genetics Part A; (2022).
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Novel genetic testing model: A collaboration between genetic counselors and nephrology; American Journal of Medical Genetics Part A; (2021).
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Phenotypic expansion of the BPTF-related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies.; American journal of medical genetics. Part A; (2021).
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Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome; American Journal of Medical Genetics, Part A; (2021).
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Nucleocytoplasmic transport of the RNA-binding protein CELF2 regulates neural stem cell fates; Cell Reports; (2021).
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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis.; Brain : a journal of neurology; (2020).
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De novo missense variants in <i>LMBRD2</i> are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features.; Journal of medical genetics; (2020).
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Three new patients with Steel syndrome and a Puerto Rican specific COL27A1 mutation; American Journal of Medical Genetics Part A; (2020).
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- English