Jeffrey Ming, MD, PhD

Jeffrey Ming, MD, PhD

Jeffrey Ming, MD, PhD, is an Attending Physician in the Division of Human Genetics at Children's Hospital of Philadelphia.

Areas of Expertise: Genetics of brain development
Locations: Main Campus
Appointments and Referrals: 1-800-TRY-CHOP (1-800-879-2467)

Education and Training

Medical School

Cornell University Medical College, New York, NY

Board Certification

American Board of Medical Genetics/Clinical Genetics
American Board of Pediatrics

Titles and Academic Titles

Attending Physician

Publications

Papers

2015

Weaver DD, Norby AR, Rosenfeld JA, Proud VK, Spangler BE, Ming JE, Chisholm E, Zackai, Lee BH, Edelmann L, Desnick RJ. Chromosome 1p36.22p36.21 duplications/ triplication causes Setleis syndrome (focal facial dermal dysplasia type III). Am J Med Genet A 167A:1061-70, 2015. Read the abstract.

2012

Srivastava K, Hu P, Solomon BD, Ming JE, Roessler E, Muenke M. Molecular analysis of the Noggin (NOG) gene in holoprosencephaly patients. Mol Genet Metab 106:241-3, 2012. Read the article.

2011

Hannibal MC, Buckingham KJ, Ng SB, Ming JE, Beck AE, McMillin MJ, Gildersleeve HI, Bigham AW, Tabor HK, Mefford HC, Cook J, Yoshiura K, Matsumoto T, Matsumoto N, Miyake N, Tonoki H, Naritomi K, Kaname T, Nagai T, Ohashi H, Kurosawa K, Hou JW, Ohta T, Liang D, Sudo A, Morris CA, Banka S, Black GC, Clayton-Smith J, Nickerson DA, Zackai EH, Shaikh TH, Donnai D, Niikawa N, Shendure J, Bamshad MJ. Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome. Am J Med Genet A 155:1511-1516, 2011. Read the article.