Physician
Medical Genetics
Dr. Duane Superneau, MD
|
|
Give Review
Duane Superneau practices Medical Genetics. He researched medicine at University of Washington School of Medicine. He has 1 awards "Regional Top Doctor". Dr. Duane Superneau is a published doctor and has 30 publications published. The lastest was: 'FG syndrome: report of three new families with linkage to Xq12-q22.1.'
Publications
- Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome.
- Initial experience with surgical treatment planning in the newly diagnosed breast cancer patient at high risk for BRCA-1 or BRCA-2 mutation.
- Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.
- Unusual cardiac malformations in conjoined twins: thoracopagus twins with conjoined pentalogy of Cantrell and an omphalopagus twin with atretic ventricles.
- Meier-Gorlin syndrome: report of eight additional cases and review.
- Sagittal craniosynostosis, Dandy-Walker malformation, and hydrocephalus: a unique multiple malformation syndrome.
- Early prenatal diagnosis: the first 100 cases of chorionic villus sampling at Ochsner Foundation Hospital.
- Peroxisomal bifunctional enzyme complex deficiency with associated retinal findings.
- Brief clinical report: a sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome.
- Neurofibromatosis, skin hemangiomas, and arterial disease.
- Comparative studies of infants with mosaic and complete triploidy: an analysis of 55 cases.
- Abnormal centromere-chromatid apposition (ACCA) and Peters'' anomaly.
- Similarity of effects--experimental hyperthermia as a teratogen and maternal febrile illness associated with oromandibular and limb defects.
- A genetic services microcomputer data base. Part II. Results and trends.
- A genetic services microcomputer data base. Part I. Design and implementation.
- Myopathy in Marinesco-Sjogren syndrome.
- Angiomas and von Recklinghausen neurofibromatosis.
- Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred.
- Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22.
- Aberrant retropharyngeal internal carotid artery in a child with spondyloepimetaphyseal dysplasia and cleft palate.
- Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?
- FG syndrome: report of three new families with linkage to Xq12-q22.1.
- Fertility and the cri du chat syndrome.
- History of the cerebrohepatorenal syndrome of Zellweger and other peroxisomal disorders.
- The Marinesco-Sjögren syndrome described a quarter of a century before Marinesco.
- Effects of education, distance and satellite clinics on the growth of genetic services.
- Clinical and behavioral characteristics in FG syndrome.
- Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
- Ventricular Fibrillation in a Patient with Pompe Disease: A Cautionary Tale.
Schools
Univ Of Wa Sch Of Med
Doctors Specialties
- Medical Genetics
Accepted Insurances
Awards
- Regional Top Doctor
Education
-
University of South Alabama -
Louisiana State University -
University of Washington School of Medicine
Hospital
-
University Health Shreveport -
Ochsner Medical Center
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1427018274 |
| Last Name Of The Provider | SUPERNEAU |
| First Name Of The Provider | DUANE |
| View All |
Similar Doctors
|
Dr. Jacqueline Kirby, PHD |
|
|
Dr. Ana R. De Aguiar, MD |
|
|
Faith S. Rickert, OT |
|
|
Johnetta R. Hall |
|
|
Dr. Michael T. Bashford, MD
 This Doctor is OpenDoctor Recommended.
|