Associate Professor, Pediatrics, Georgetown University School of Medicine

Medical Genetics

Nina Scribanu works in the field of Medical Genetics. She went to NYU School of Medicine. Dr. Nina Scribanu is a published doctor and has 14 publications published. The lastest was: 'Proceedings: The syndrome of aplasia cutis congenita with terminal transverse defects of limbs.'

Publications

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• Y-position cysteine substitution in type I collagen (alpha1(I) R888C/p.R1066C) is associated with osteogenesis imperfecta/Ehlers-Danlos syndrome phenotype.
• The microcephaly-lymphoedema syndrome: report of an additional family.
• Chorioretinal lacuna in the amniotic band syndrome.
• Familial Wolf-Hirschhorn syndrome associated with Rieger anomaly of the eye.
• The Weissenbacher-Zweymüller phenotype in the neonatal period as an expression in the continuum of manifestations of the hereditary arthro-ophthalmopathies.
• Schwartz-Jampel syndrome: a case report. Stimulatory effect of calcium and A23187 calcium ionophore for protein synthesis in muscle cell cultures.
• The syndrome of ring chromosome 12.
• Stability and comparability of intellectual measures for cerebral-palsied preschoolers.
• Proceedings: The syndrome of aplasia cutis congenita with terminal transverse defects of limbs.
• Familial syndrome with dystonia, neural deafness, and possible intellectual impairment: clinical course and pathological findings.
• Observations on patients with neural-tube defects in a metropolitan hospital clinic: an epidemiological history.
• The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs.
• Platelet serotonin of hyperactive school age boys.

Schools

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• Institute of Medicine And Pharmacy quotCarol Davilaquot

• NyuBellevue Mc

• Bellevue Hospital Center

• Georgetown University

Doctors Specialties

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• Clinical Genetics
• Pediatrics
• Medical Genetics

Accepted Insurances

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Education

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• NYU School of Medicine

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