Roger Stevenson is a Medical Genetics provider in Greenwood, South Carolina. Dr. Stevenson is rated as an Advanced provider by MediFind in the treatment of Phocomelia. His top areas of expertise are Micrognathia, Phocomelia, VACTERL Association, and FG Syndrome. Dr. Stevenson is currently accepting new patients.

Deborah Krakow is a Medical Genetics specialist and an Obstetrics and Gynecologist in Los Angeles, California. Dr. Krakow is rated as an Advanced provider by MediFind in the treatment of Phocomelia. Her top areas of expertise are Osteogenesis Imperfecta, Acromicric Dysplasia, Chondrodystrophy, and Spondyloepimetaphyseal Dysplasia Strudwick Type.

Jessica Tenney is a Medical Genetics provider in San Francisco, California. Dr. Tenney is rated as an Advanced provider by MediFind in the treatment of Phocomelia. Her top areas of expertise are Acrofacial Dysostosis Catania Type, Phocomelia, Acromicric Dysplasia, and Acrofacial Dysostosis Nager Type.

Dr. Ian Daniel Krantz, MD, is a renowned physician specializing in Genetics and Pediatrics. He currently sees patients at Cohen Children's Medical Center (CCMC) and Northwell Health Physician Partners Medical Genetics. Dr. Krantz holds certifications in Clinical Genetics, Cytogenetics, and Pediatrics from the American Board of Medical Genetics and the American Board of Pediatrics, respectively.Dr. Krantz completed his BFA at Concordia University in Montreal and his MD at Sackler School of Medicine (Tel Aviv University). He completed his residency in Medical Genetics at Children's Hospital of Philadelphia and his residency in Pediatrics at New York University Medical Center.With an impressive set of academic and administrative titles, Dr. Krantz serves as the Division Chief of Pediatric Genetics and Genomics at Cohen Children's Medical Center and is the System Vice President for Pediatric Genetics at Northwell Health. Additionally, he holds the position of Professor at the Zucker School of Medicine at Northwell Health.Dr. Krantz is recognized for his clinical expertise in isolated and syndromic forms of congenital birth differences and developmental diagnoses, including syndromic and non-syndromic autism. He has a special interest in the genetics of hearing loss and focused expertise in Cornelia de Lange Syndrome, Pallister-Killian syndrome, Alagille syndrome, CHOPS syndrome, among others.Dr. Krantz's research is dedicated to identifying and characterizing the molecular etiology of syndromic and non-syndromic developmental diagnoses. His research lab has made significant contributions in the field, discovering new disease genes and shedding light on critical molecular pathways involved in human developmental disorders.Driven by his commitment to advancing patient care, Dr. Krantz has been at the forefront of integrating genomic technologies into the clinical setting. He has implemented rapid genome sequencing into the NICU and CICU and established biobanks and biorepositories to further research efforts. Through his work, he aims to understand the impact of complex diagnostic information on clinicians and families involved.With his extensive expertise and dedication to advancing genetic research and patient care, Dr. Krantz continues to make significant contributions to the field of Pediatrics and Genetics. Dr. Krantz is rated as an Experienced provider by MediFind in the treatment of Phocomelia. His top areas of expertise are Cornelia De Lange Syndrome, Pallister-Killian Mosaic Syndrome, Mosaicism, and KBG Syndrome.

Angela Lin is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Lin is rated as an Experienced provider by MediFind in the treatment of Phocomelia. Her top areas of expertise are Myhre Syndrome, Turner Syndrome, Intersex, Undescended Testicle, and Hormone Replacement Therapy (HRT). Dr. Lin is currently accepting new patients.

Ethylin Jabs is a Medical Genetics specialist and a Pediatrics provider in Rochester, Minnesota. Dr. Jabs is rated as an Experienced provider by MediFind in the treatment of Phocomelia. Her top areas of expertise are Craniosynostosis, Beare-Stevenson Cutis Gyrata Syndrome, Crouzon Syndrome, and Roberts Syndrome. Dr. Jabs is currently accepting new patients.

Matthew Deardorff is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Deardorff is rated as an Experienced provider by MediFind in the treatment of Phocomelia. His top areas of expertise are Cornelia De Lange Syndrome, Coffin-Siris Syndrome, Mosaicism, and Beckwith-Wiedemann Syndrome.

Lorenzo Botto is a Medical Genetics specialist and a Pediatrics provider in Salt Lake City, Utah. Dr. Botto is rated as an Experienced provider by MediFind in the treatment of Phocomelia. His top areas of expertise are Gastroschisis, Omphalocele, Increased Head Circumference, and Brachydactyly Mononen Type. Dr. Botto is currently accepting new patients.

Uta Francke is a Medical Genetics specialist and a Pediatrics provider in Stanford, California. Dr. Francke is rated as an Experienced provider by MediFind in the treatment of Phocomelia. Her top areas of expertise are Roberts Syndrome, Myeloproliferative Neoplasms (MPN), Chromosome 7p Deletion, and Phocomelia.

David Beck is a Medical Genetics specialist and a Rheumatologist in New York, New York. Dr. Beck is rated as an Experienced provider by MediFind in the treatment of Phocomelia. His top areas of expertise are VEXAS Syndrome, Relapsing Polychondritis, Hypotonia, and Polyarteritis Nodosa.