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TERENCE ROUSSEAU, DO
DO
Family Medicine Physician
NPI: 1770795049Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
4554(AZ)A-1784-13(NM)
Research & Publications (19)
Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20.
PMID 19670346·Prenat Diagn·2009
5-case
Contribution of three-dimensional computed tomography in prenatal diagnosis of lethal infantile cortical hyperostosis (Caffey disease).
PMID 19455587·Prenat Diagn·2009
5-case
BODIPY derivatives as donor materials for bulk heterojunction solar cells.
PMID 19294258·Chem Commun (Camb)·2009
8-other
[Liveborn birth-weight of single and uncomplicated pregnancies between 28 and 42 weeks of gestation from Burgundy perinatal network].
PMID 18355985·J Gynecol Obstet Biol Reprod (Paris)·2008
8-other
Syndromic encephalocele in a fetal case with a 1p35-pter deletion and a 14q32-qter duplication inherited from a maternal balanced translocation.
PMID 17385797·Prenat Diagn·2007
5-case
A new osteochondrodysplasia with severe osteopenia, preaxial polydactyly, clefting and dysmorphic features resembling filamin-related disorders.
PMID 17009344·Prenat Diagn·2006
5-case
Fetal serum beta2-microglobulin as a marker for fetal infectious diseases.
PMID 16652403·Prenat Diagn·2006
8-other
Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome.
PMID 16059936·Am J Med Genet A·2005
5-case
Interest of F-18 fluorodeoxyglucose positron emission tomography in the evaluation of vaginal malignant melanoma.
PMID 15582002·Gynecol Oncol·2004
5-case
Prenatal overgrowth and mosaic trisomy 15q25-qter including the IGF1 receptor gene.
PMID 15164417·Prenat Diagn·2004
5-case
Fetal serum ss2-microglobulin and cystatin C in the prediction of post-natal renal function in bilateral hypoplasia and hyperechogenic enlarged kidneys.
PMID 15164404·Prenat Diagn·2004
4-observational
Recurrence of achondrogenesis type II within the same family: evidence for germline mosaicism.
PMID 15054848·Am J Med Genet A·2004
5-case
Hypomandibular faciocranial dysostosis in consanguineous parents revealed by ultrasound prenatal diagnosis.
PMID 12210581·Prenat Diagn·2002
5-case
Prenatal diagnosis and intrafamilial clinical heterogeneity of Fraser syndrome.
PMID 12210578·Prenat Diagn·2002
5-case
Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephaly.
PMID 11438951·Prenat Diagn·2001
5-case
[Voluntary interruption of pregnancy: comparative study between 1982 and 1996 in the main center of Côte d'Or. Study of women having repeat voluntary interruption of pregnancy].
PMID 11300045·Gynecol Obstet Fertil·2001
4-observational
Severe fetal cytomegalic inclusion disease after documented maternal reactivation of cytomegalovirus infection during pregnancy.
PMID 10740207·Prenat Diagn·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
Via practice · 2 locations total
- Address
- 1231 ZUNI ST
HOBBS, NM 88240 - Phone
- (602) 571-3976
Quick Facts
- NPI
- 1770795049
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 19
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