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MARLIS KIRCHHOFF, PH.D.
PH.D.
Clinical Psychologist
NPI: 1770153801Individual
Specialties, Licenses & Credentials
Clinical PsychologistPrimary
Psychologist — Clinical
Code: 103TC0700X
PSY-203377(ID)PY60677390(WA)
Research & Publications (20)
Phenotype and 244k array-CGH characterization of chromosome 13q deletions: an update of the phenotypic map of 13q21.1-qter.
PMID 19363806·Am J Med Genet A·2009
4-observational
A new microduplication syndrome encompassing the region of the Miller-Dieker (17p13 deletion) syndrome.
PMID 19520700·J Med Genet·2009
5-case
Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy.
PMID 19054018·Clin Genet·2009
5-case
Facial asymmetry associated with small and large intestinal atresia, and ipsilateral malformations of eye, skin, and extremities.
PMID 18388783·Clin Dysmorphol·2008
5-case
Multiplex ligation-dependent probe amplification (MLPA) in prenatal diagnosis-experience of a large series of rapid testing for aneuploidy of chromosomes 13, 18, 21, X, and Y.
PMID 19003800·Prenat Diagn·2008
8-other
Advanced medical simulation applications for emergency medicine microsystems evaluation and training.
PMID 18828832·Acad Emerg Med·2008
8-other
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.
PMID 17480035·Hum Mutat·2007
8-other
Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences.
PMID 17318843·Am J Med Genet A·2007
5-case
Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata.
PMID 17351355·Clin Dysmorphol·2007
5-case
Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.
PMID 17392702·Eur J Hum Genet·2007
8-other
Additional chromosomal abnormalities in patients with a previously detected abnormal karyotype, mental retardation, and dysmorphic features.
PMID 16955412·Am J Med Genet A·2006
5-case
Twins with mental retardation and an interstitial deletion 7q34q36.2 leading to the diagnosis of long QT syndrome.
PMID 16470702·Am J Med Genet A·2006
5-case
[The significance of cataract surgery and balance function of the elderly].
PMID 16545218·Ugeskr Laeger·2006
8-other
Flow cytometric DNA index, G-band karyotyping, and comparative genomic hybridization in detection of high hyperdiploidy in childhood acute lymphoblastic leukemia.
PMID 16679935·J Pediatr Hematol Oncol·2006
4-observational
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation.
PMID 17124407·Cytogenet Genome Res·2006
8-other
Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplification.
PMID 16278905·Am J Med Genet A·2005
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
- 305 TROY MALL LANE WASHINGTON STATE UNIV
PULLMAN, WA 99164 - Phone
- (509) 335-3935
Quick Facts
- NPI
- 1770153801
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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