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HAROLD HOYME, M.D.
M.D.
NPI: 1518077908Individual
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
7006(SD)
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
7006(SD)
Research & Publications (20)
Elements of morphology: standard terminology for the head and face.
PMID 19125436·Am J Med Genet A·2009
8-other
Developmental pathogenesis of short palpebral fissure length in children with fetal alcohol syndrome.
PMID 19350654·Birth Defects Res A Clin Mol Teratol·2009
8-other
Design, construction, and testing of a stereo-photogrammetric tool for the diagnosis of fetal alcohol syndrome in infants.
PMID 19336298·IEEE Trans Med Imaging·2009
8-other
Automated diagnosis of fetal alcohol syndrome using 3D facial image analysis.
PMID 18713153·Orthod Craniofac Res·2008
8-other
Progressive and symmetric supraorbital hyperostosis with bony and soft tissue overgrowth in an Ethiopian female: a newly recognized overgrowth syndrome?
PMID 18241057·Am J Med Genet A·2008
5-case
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
PMID 18245432·Pediatrics·2008
8-other
Impaired eyeblink conditioning in children with fetal alcohol syndrome.
PMID 18162064·Alcohol Clin Exp Res·2008
8-other
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.
PMID 18000912·Am J Med Genet A·2007
5-case
Unique facial features distinguish fetal alcohol syndrome patients and controls in diverse ethnic populations.
PMID 17850644·Alcohol Clin Exp Res·2007
4-observational
The epidemiology of fetal alcohol syndrome and partial FAS in a South African community.
PMID 17127017·Drug Alcohol Depend·2007
8-other
22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay.
PMID 17926345·Am J Med Genet C Semin Med Genet·2007
6-review
Relationship between dysmorphic features and general cognitive function in children with fetal alcohol spectrum disorders.
PMID 18000897·Am J Med Genet A·2007
7-preclinical
Systemic hyalinosis: a distinctive early childhood-onset disorder characterized by mutations in the anthrax toxin receptor 2 gene (ANTRX2).
PMID 17043134·Pediatrics·2006
5-case
Nablus mask-like facial syndrome is caused by a microdeletion of 8q detected by array-based comparative genomic hybridization.
PMID 16691576·Am J Med Genet A·2006
5-case
Triplication of 8p22-8p23 in a patient with features similar to Kabuki syndrome.
PMID 16353235·Am J Med Genet A·2006
5-case
Fetal alcohol spectrum disorders in Finland: clinical delineation of 77 older children and adolescents.
PMID 16353236·Am J Med Genet A·2006
8-other
Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
PMID 16532473·Am J Med Genet A·2006
5-case
Unilateral aquagenic wrinkling of the palms associated with aspirin intake.
PMID 17179009·Arch Dermatol·2006
5-case
Fetal alcohol syndrome epidemiology in a South African community: a second study of a very high prevalence area.
PMID 16331845·J Stud Alcohol·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1501 N CAMPBELL AVE
TUCSON, AZ 85724 - Phone
- (520) 626-2182
Quick Facts
- NPI
- 1518077908
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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