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NOEL ROBIN, MD
MD
Endocrinology, Diabetes & Metabolism Physician
NPI: 1962413948Individual
Specialties, Licenses & Credentials
Endocrinology, Diabetes & Metabolism PhysicianPrimary
Internal Medicine — Endocrinology, Diabetes & Metabolism
Code: 207RE0101X
061279(CT)
Research & Publications (20)
Genetic and reproductive knowledge among adolescents and adults with cystic fibrosis.
PMID 18574307·Chest·2008
8-other
Amniotic constriction band: a multidisciplinary assessment of etiology and clinical presentation.
PMID 19571071·J Bone Joint Surg Am·2009
8-other
Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1.
PMID 19213029·Am J Med Genet A·2009
5-case
Isolated facial hemihyperplasia: manifestation of Beckwith-Wiedemann syndrome.
PMID 18216702·J Craniofac Surg·2008
5-case
The use of role-play to enhance medical student understanding of genetic counseling.
PMID 18813131·Genet Med·2008
8-other
Proximal versus distal cues to smoke: the effects of environments on smokers' cue-reactivity.
PMID 18540780·Exp Clin Psychopharmacol·2008
8-other
Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?
PMID 18680190·Am J Med Genet A·2008
8-other
Unanticipated difficult airway management in anaesthetised patients: a prospective study of the effect of mannequin training on management strategies and skill retention.
PMID 18336486·Anaesthesia·2008
8-other
The use by Alabama pediatricians of genetics consultation in the evaluation of developmental delay.
PMID 18203192·Am J Med Genet A·2008
8-other
Caring for adults with pediatric genetic diseases: a growing need.
PMID 18025925·Curr Opin Pediatr·2007
8-other
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).
PMID 17603794·Am J Med Genet A·2007
5-case
A genetic model for cloacal exstrophy, the extreme cloacal malformation.
PMID 18947738·J Pediatr Urol·2007
8-other
Pediatric otolaryngologists' use of genetic testing.
PMID 17372079·Arch Otolaryngol Head Neck Surg·2007
8-other
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation.
PMID 17036343·Am J Med Genet A·2006
8-other
It does matter: the importance of making the diagnosis of a genetic syndrome.
PMID 17099356·Curr Opin Pediatr·2006
8-other
The multidisciplinary evaluation and management of cleft lip and palate.
PMID 17100032·South Med J·2006
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 30 SHELBURNE RD, DEPARTMENT OF MEDICINE
STAMFORD, CT 06902 - Phone
- (203) 276-7485
Quick Facts
- NPI
- 1962413948
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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