The 20 Best Chromosome 13q Deletion Doctors Near Me in Minnesota, US

Find the Top Chromosome 13q Deletion Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 5 doctor with experience in Chromosome 13q Deletion near Minnesota, US. Of these, 4 are Experienced and 1 are Advanced.

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5 providers found
    Advanced in Chromosome 13q Deletion
    Medical Genetics
    Advanced in Chromosome 13q Deletion
    Medical Genetics
    Referral may be required

    Children's Specialty Clinic - Genetics

    2525 Chicago Avenue, 
    Minneapolis, MN 
    Languages Spoken:
    English, Spanish
    Accepting New Patients

    Marcelo Vargas is a Medical Genetics provider practicing medicine in Minneapolis, Minnesota. Dr. Vargas is rated as an Advanced provider by MediFind in the treatment of Chromosome 13q Deletion. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Chromosome 13q Deletion, Cat Eye Syndrome, Branchio-Oculo-Facial Syndrome (BOFS), and Chromosome 2 Uniparental Disomy. Dr. Vargas is board certified in Pediatrics, 2011, Clinical Biochemical Genetics, American Board Of Medical Genetics And Genomics,2024, Clinical Genetics (MD), American Board Of Pediatrics, and 2015. Dr. Vargas is currently accepting new patients.

    Experienced in Chromosome 13q Deletion
    Pediatrics | Medical Genetics
    Experienced in Chromosome 13q Deletion
    Pediatrics | Medical Genetics
    Referral may be required

    M Health Fairview Explorer Pediatric Specialty Clinic

    2450 Riverside Avenue, Floor 12, 
    Minneapolis, MN 
    Languages Spoken:
    English, Hindi, Malay, Malayalam, Malayan, Tamil
    Accepting New Patients
    Offers Telehealth

    Nishitha Pillai is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Minneapolis, Minnesota. Dr. Pillai is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Deletion. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Hartnup Disease, Pompe Disease, Multiple Sulfatase Deficiency, and Hardikar Syndrome. Dr. Pillai is board certified in Medical Biochemical Genetics: American Board Of Medical Genetics And Genomics, 2019, Clinical Genetics And Genomics: American Board Of Medical Genetics And Genomics, 2019, and Pediatrics: American Board Of Pediatrics, 2014. Dr. Pillai is currently accepting new patients.

    Experienced in Chromosome 13q Deletion
    Pediatrics | Medical Genetics
    Experienced in Chromosome 13q Deletion
    Pediatrics | Medical Genetics
    Referral may be required
    2450 Riverside Ave, 
    Minneapolis, MN 
    Languages Spoken:
    English, Hindi
    Accepting New Patients

    Anjali Aggarwal is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Minneapolis, Minnesota. Dr. Aggarwal is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Deletion. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Marshall-Smith Syndrome, Multiple Synostoses Syndrome 1, Hardikar Syndrome, Osteotomy, and Colonoscopy. Dr. Aggarwal is board certified in Medical Biochemical Genetics: American Board Of Medical Genetics And Genomics, 2019 and Clinical Genetics And Genomics: American Board Of Medical Genetics And Genomics, 2019. Dr. Aggarwal is currently accepting new patients.

    Learn about our expert tiers
    Experienced in Chromosome 13q Deletion
    Medical Genetics
    Experienced in Chromosome 13q Deletion
    Medical Genetics
    Referral may be required

    Children's Specialty Clinic - Genetics

    2525 Chicago Avenue, 
    Minneapolis, MN 
    Languages Spoken:
    English, Filipino
    Accepting New Patients

    Noelle Fabie is a Medical Genetics provider practicing medicine in Minneapolis, Minnesota. Dr. Fabie is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Deletion. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Micrognathia, Culler Jones Syndrome, Oculodentodigital Dysplasia Dominant, and Townes-Brocks Syndrome. Dr. Fabie is board certified in Pediatrics, Clinical Genetics (MD), American Board Of Medical Genetics And Genomics, and American Board Of Pediatrics. Dr. Fabie is currently accepting new patients.

    Experienced in Chromosome 13q Deletion
    Medical Genetics
    Experienced in Chromosome 13q Deletion
    Medical Genetics
    Referral may be required

    Children's Specialty Clinic - Genetics

    2525 Chicago Avenue, 
    Minneapolis, MN 
    Languages Spoken:
    English
    Accepting New Patients

    Amy Lebedoff is a Medical Genetics provider practicing medicine in Minneapolis, Minnesota. Dr. Lebedoff is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Deletion. Her clinical expertise encompasses Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Increased Head Circumference, and Cantu Syndrome. Dr. Lebedoff is board certified in Pediatrics, American Board Of Medical Genetics And Genomics,2021, Clinical Genetics (MD), 2018, and American Board Of Pediatrics. Dr. Lebedoff is currently accepting new patients.

    Showing 1-5 of 5

    Last Updated: 09/26/2026

    What is the definition of Chromosome 13q Deletion?

    Chromosome 13q deletion is a chromosome abnormality that occurs when there is a missing (deleted) copy of genetic material on the long arm (q) of chromosome 13. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with Chromosome 13q deletion include developmental delay, intellectual disability, behavioral problems and distinctive facial features. Chromosome testing of both parents can provide more information on whether or not the deletion was inherited. In most cases, parents do not have any chromosomal anomaly. However, sometimes one parent is found to have a balanced translocation, where a piece of a chromosome has broken off and attached to another one with no gain or loss of genetic material. The balanced translocation normally does not cause any signs or symptoms, but it increases the risk for having an affected child with a chromosomal anomaly like a deletion.

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