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STEPHEN LANGLOIS, D.M.D.
D.M.D.
General Practice Dentistry
NPI: 1487872354Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
1871(NH)
Research & Publications (20)
An interprofessional education session for first-year health science students.
PMID 19657495·Am J Pharm Educ·2009
8-other
Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols.
PMID 19609942·Prenat Diagn·2009
8-other
A novel de novo 1.1 Mb duplication of 17q21.33 associated with cognitive impairment and other anomalies.
PMID 19449402·Am J Med Genet A·2009
5-case
Diagnosing chromosomal abnormalities from "big" to "small" with molecular cytogenetic technology.
PMID 19604422·J Obstet Gynaecol Can·2009
6-review
An evaluation of the decision-making process regarding amniocentesis following a screen-positive maternal serum screen result.
PMID 19242922·Prenat Diagn·2009
8-other
Sonic hedgehog guides axons through a noncanonical, Src-family-kinase-dependent signaling pathway.
PMID 19447091·Neuron·2009
4-observational
Carrier screening for thalassemia and hemoglobinopathies in Canada.
PMID 19038079·J Obstet Gynaecol Can·2008
6-review
Caveolin-1 and -2 interact with connexin43 and regulate gap junctional intercellular communication in keratinocytes.
PMID 18162583·Mol Biol Cell·2008
7-preclinical
New molecular techniques for the prenatal detection of chromosomal aneuploidy.
PMID 18644185·J Obstet Gynaecol Can·2008
8-other
[Efficacy of percutaneous laser disc decompression for radiculalgia due to lumbar disc hernia (149 patients)].
PMID 17662570·Presse Med·2007
3-trial
Connexin levels regulate keratinocyte differentiation in the epidermis.
PMID 17693411·J Biol Chem·2007
7-preclinical
RETIRED: Mid-trimester amniocentesis fetal loss rate.
PMID 17623573·J Obstet Gynaecol Can·2007
6-review
Membrane-type 1 matrix metalloproteinase stimulates cell migration through epidermal growth factor receptor transactivation.
PMID 17541067·Mol Cancer Res·2007
7-preclinical
Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children.
PMID 17545556·J Med Genet·2007
5-case
Renal-hepatic-pancreatic dysplasia: an autosomal recessive condition that is not linked to the PKHD1 gene on chromosome 6p21.1-p12.
PMID 17593545·Am J Med Genet A·2007
5-case
De novo mutation of the DHCR7 gene in a fetus with severe Smith-Lemli-Opitz (or RSH) syndrome.
PMID 17595012·Am J Med Genet A·2007
5-case
Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data.
PMID 17910767·BMC Bioinformatics·2007
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
- 765 S MAIN ST, SUITE 102
MANCHESTER, NH 03102 - Phone
- (603) 644-3368
Quick Facts
- NPI
- 1487872354
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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