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JOE HOO, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1821022849Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
195689(NY)
Research & Publications (17)
Two sibs with brachyolmia type Hobaek: five year follow-up through puberty.
PMID 12476457·Am J Med Genet A·2003
8-other
Distal 3p deletion is not necessarily associated with dysmorphic features or psychomotor delay.
PMID 18203205·Am J Med Genet A·2008
8-other
"Zwilling" versus "Tai Chi" configuration of double-sized ring chromosome.
PMID 17352391·Am J Med Genet A·2007
5-case
Succinate dehydrogenase deficiency associated with dilated cardiomyopathy and ventricular noncompaction.
PMID 17082968·Eur J Pediatr·2007
5-case
Desbuquois syndrome in three sisters with significantly different lengths of survival.
PMID 16642505·Am J Med Genet A·2006
5-case
Difficulty in recognizing multiple sulfatase deficiency in an infant.
PMID 16510683·Pediatrics·2006
5-case
Karyotype-phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficit.
PMID 16411192·Am J Med Genet A·2006
5-case
Familial hyper- and hypopigmentation with age-related pattern change.
PMID 15551335·Am J Med Genet A·2005
8-other
Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype.
PMID 15521982·Clin Genet·2004
5-case
Is brachydactyly type Ballard a variant of brachydactyly type E?
PMID 15266625·Am J Med Genet A·2004
5-case
New syndrome characterized by sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay.
PMID 11343342·Am J Med Genet·2001
5-case
Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: exclusion of the Aarskog (FGD1) gene as a candidate gene.
PMID 11241498·Am J Med Genet·2001
8-other
Spontaneous coronary artery dissection presenting as acute myocardial infarction.
PMID 10800297·J Natl Med Assoc·2000
5-case
Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31.
PMID 10797443·Am J Med Genet·2000
5-case
Anodontia of permanent teeth (OMIM # 206780) and pegged/missing maxillary lateral incisors (OMIM # 150400) in the same family.
PMID 10710232·Am J Med Genet·2000
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 750 E ADAMS ST
SYRACUSE, NY 13210 - Phone
- (315) 464-2096
Quick Facts
- NPI
- 1821022849
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 17
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