The 20 Best Beckwith-Wiedemann Syndrome Doctors Near Me in Phoenix, AZ
Find the Top Beckwith-Wiedemann Syndrome Experts and Specialists
Phoenix Children's Hospital - Genetics
Theresa Grebe is a Pediatrics provider practicing medicine in Phoenix, Arizona. Dr. Grebe is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 96 other conditions, according to our data. Her clinical expertise encompasses Chromosome 6 Uniparental Disomy, Temple Syndrome, Congenital Bowing of Long Bones, and DiGeorge Syndrome. Dr. Grebe is board certified in Medical Genetics And Genomics Clin Genetics & Genomic. Dr. Grebe is currently accepting new patients.
John Baker is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Phoenix, Arizona. Dr. Baker is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Chromosome 6 Uniparental Disomy, Chromosome 11 Uniparental Disomy, and Temple Syndrome. Dr. Baker is currently accepting new patients.
Phoenix Children's Hospital - Genetics
Derek Neilson is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Phoenix, Arizona. Dr. Neilson is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 25 other conditions, according to our data. His clinical expertise encompasses Ehlers-Danlos Syndrome (EDS), Vascular Ehlers-Danlos Syndrome (VEDS), Brittle Cornea Syndrome, and Chromosome 6 Uniparental Disomy. Dr. Neilson is board certified in Medical Genetics And Genomics Clin Genetics & Genomic.
Phoenix Children's Hospital
Jasmine Knoll is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Phoenix, Arizona. Dr. Knoll is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 8 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Multiple Sulfatase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts. Dr. Knoll is currently accepting new patients.
Last Updated: 04/28/2026
