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SUZANNE BRADDOCK, M.D.
M.D.
Specialist
NPI: 1770522161Individual
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
14695(NE)
Research & Publications (19)
A new recessive syndrome with VATER-like defects, pulmonary hypertension, abnormal ears, blue sclera, laryngeal webs, and persistent growth deficiency.
PMID 14556254·Am J Med Genet A·2003
5-case
Tertiary trisomy due to a reciprocal translocation of chromosomes 5 and 21 in a four-generation family.
PMID 10861659·Am J Med Genet·2000
5-case
An unusual presentation of Ehlers-Danlos syndrome vascular type with deep vein thrombosis: a case for multidisciplinary management.
PMID 19248182·Am J Med Genet A·2009
5-case
Development and validation of a measure of dysmorphology: useful for autism subgroup classification.
PMID 18383511·Am J Med Genet A·2008
4-observational
Disruption of neurexin 1 associated with autism spectrum disorder.
PMID 18179900·Am J Hum Genet·2008
8-other
The face of Joubert syndrome: a study of dysmorphology and anthropometry.
PMID 18000967·Am J Med Genet A·2007
8-other
Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.
PMID 17850629·Clin Genet·2007
8-other
Linking Antley-Bixler syndrome and congenital adrenal hyperplasia: a novel case of P450 oxidoreductase deficiency.
PMID 16906539·Am J Med Genet A·2006
5-case
Further delineation of Kabuki syndrome in 48 well-defined new individuals.
PMID 15690370·Am J Med Genet A·2005
8-other
Potential modifier role of the R618Q variant of proalpha2(I)collagen in type I collagen fibrillogenesis: in vitro assembly analysis.
PMID 15172002·Mol Genet Metab·2004
8-other
Retinal hemorrhages in an 8-year-old child: an uncommon presentation of abusive injury.
PMID 14758311·Pediatr Emerg Care·2004
5-case
Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B.
PMID 12784289·Am J Med Genet A·2003
8-other
Perioperative care of the child with the Johanson-Blizzard syndrome.
PMID 12535044·Paediatr Anaesth·2003
5-case
Postmarketing surveillance for human teratogenicity: a model approach.
PMID 11745831·Teratology·2001
4-observational
Establishment of normative data for orbital and nasal soft-tissue measurements among Filipino children.
PMID 11572246·J Craniofac Surg·2001
8-other
Septo-optic dysplasia as a manifestation of valproic acid embryopathy.
PMID 11460259·Teratology·2001
5-case
Blepharoptosis and central nervous system abnormalities in combined valproate and hydantoin embryopathy.
PMID 10674735·Ophthalmic Plast Reconstr Surg·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 7911 W CENTER RD
OMAHA, NE 68124 - Phone
- (402) 390-0333
Quick Facts
- NPI
- 1770522161
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 19
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