Back to Search
JEFFREY INNIS, MD
MD
Clinical Molecular Genetics Physician
NPI: 1053321679Individual
Specialties, Licenses & Credentials
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
4301058671(MI)
Medical Genetics — Clinical Molecular Genetics
Code: 207SG0203X
ME152778(FL)
Research & Publications (20)
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
PMID 19372089·J Med Genet·2009
8-other
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
PMID 19029900·Nat Genet·2008
8-other
Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome.
PMID 17935235·Am J Med Genet A·2007
7-preclinical
A mouse transgene drives embryonic dorsal posterior commissure expression.
PMID 17549599·Transgenic Res·2007
4-observational
Craniofacial dyssynostosis in two boys with apparently normal cognitive development.
PMID 16691590·Am J Med Genet A·2006
5-case
Description and genetic mapping of Polypodia: an X-linked dominant mouse mutant with ectopic caudal limbs and other malformations.
PMID 16964440·Mamm Genome·2006
7-preclinical
A group 13 homeodomain is neither necessary nor sufficient for posterior prevalence in the mouse limb.
PMID 16806154·Dev Biol·2006
7-preclinical
Candidate downstream regulated genes of HOX group 13 transcription factors with and without monomeric DNA binding capability.
PMID 15733672·Dev Biol·2005
7-preclinical
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
- 1500 E MEDICAL CENTER DR
ANN ARBOR, MI 48109 - Phone
- (734) 936-4000
Quick Facts
- NPI
- 1053321679
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 2
- Publications
- 20
Are you this provider?
Claim Your Profile