Dr. Joe J Hoo MD
Geneticist | Clinical Genetics (M.D.)
750 E Adams St Syracuse NY, 13210About
Dr. Joe Hoo practices Genetic Medicine in Syracuse, NY. As a geneticist, Dr. Hoo performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Hoo carries out studies, tests, and counsels patients with genetic diseases.
Education and Training
Philipps-Univ, Fak Human Med, Marburg, Germany 1972
Philipps-Universitaet Marburg, Fachbereich Medizin 1972
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Mapping of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature to Xq12-q21.31.
- Anodontia of permanent teeth (OMIM # 206780) and pegged/missing maxillary lateral
- Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31.
- 12P trisomy: a syndrome?
- Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: exclusion of the Aarskog (FGD1) gene as a candidate gene.
- New syndrome characterized by sparse hair, prominent nose, small mouth,
- Two sibs with brachyolmia type Hobaek: five year follow-up through puberty.
- Twin brothers with MIDAS syndrome and XX karyotype.
- Confirmation of centromeric fusion in 7p/1q translocation associated with myelodysplastic syndrome.
- Is brachydactyly type Ballard a variant of brachydactyly type E?
- Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype.
- A new chromosome 9 variant: an extra band within the 9qh region.
- Karyotype-phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficit.
- A TNNI2 mutation in a family with distal arthrogryposis type 2B.
- Difficulty in recognizing multiple sulfatase deficiency in an infant.
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