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ALFRED MONCLA, MD
MD
Obstetrics & Gynecology Physician
NPI: 1013148063Individual
Specialties, Licenses & Credentials
Research & Publications (20)
A cluster of translocation breakpoints in 2q37 is associated with overexpression of NPPC in patients with a similar overgrowth phenotype.
PMID 17676597·Hum Mutat·2007
5-case
Polymorphisms in the C-terminal domain of MECP2 in mentally handicapped boys: implications for genetic counselling.
PMID 11896461·Eur J Hum Genet·2002
8-other
Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia.
PMID 19635726·J Med Genet·2010
7-preclinical
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
PMID 19578037·J Med Genet·2010
8-other
SOS1 and PTPN11 mutations in five cases of Noonan syndrome with multiple giant cell lesions.
PMID 19352411·Eur J Hum Genet·2009
5-case
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion.
PMID 19073947·Neurology·2009
5-case
Identification of TRAF6-dependent NEMO polyubiquitination sites through analysis of a new NEMO mutation causing incontinentia pigmenti.
PMID 17728323·Hum Mol Genet·2007
5-case
Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome.
PMID 17439480·Eur J Neurosci·2007
7-preclinical
Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.
PMID 17264869·Eur J Hum Genet·2007
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
- 1141 N ROAD ST, SUITE I
ELIZABETH CITY, NC 27909 - Phone
- (252) 338-0101
Quick Facts
- NPI
- 1013148063
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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