Medical Director American College of Medical Genetics and Genomics
Medical Genetics
Dr. David B. Flannery, MD
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Doctor David B. Flannery, MD practices Medical Genetics. He attended Emory University School of Medicine. Emory University School of Medicine is ranked 23/42 in Research/PrimaryCare. He received awards:"Regional Top Doctor". David B. Flannery, MD is also published. He has 27 publications published. The lastest publication: "Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited marker.' David Flannery accepts all Medicare patients.
Publications
- Complete monosomy 21 confirmed by FISH and array-CGH.
- Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.
- Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features.
- Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
- Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple co...
- Facial dysmorphologic and skeletal cephalometric findings associated with conotruncal cardiac anomalies. off.
- The Schinzel-Giedion syndrome.
- Nondisjunction in Down syndrome.
- Nucleolar organizer region variants as a risk factor for Down syndrome.
- 3-M syndrome.
- Syndrome of imperforate oropharynx with costovertebral and auricular anomalies.
- Dermatoglyphics in Börjeson-Forssman-Lehmann syndrome.
- Verification of the fetal valproate syndrome phenotype.
- An apparent de novo terminal deletion of chromosome 2 (pter----p24:).
- Unexplained indirect hyperbilirubinemia, hypercholesterolemia, and spur cell formation in two male siblings: a variant of cholesteryl ester deposition.
- The possible role of homeotic genes in the causation of malformations in monozygotic twins.
- Joubert syndrome: early diagnosis by recognition of the behavioral phenotype and confirmation by cranial sonography.
- Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.
- Johanson-Blizzard syndrome and hypopituitarism.
- Microdeletion of chromosome sub-band 2q37.3 in two patients with abnormal situs viscerum.
- Hypertrichosis cubiti.
- Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism.
- Frontofacionasal dysplasia.
- Ring chromosome 5.
- Packed red cell transfusion does not compromise chromosome analysis in newborns.
- Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited marker.
Schools
Emory Univ Sch Of Med
Emory University
University Of Virginia
Med College Va
Doctors Specialties
- Clinical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
Awards
- Regional Top Doctor
Education
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Virginia Commonwealth University Health System -
University of Virginia -
Emory University School of Medicine
Hospital
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Georgia Regents Medical Center
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