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CLARISSA FAUTH, MD

MD

Anatomic Pathology Physician

NPI: 1336379437Individual

Specialties, Licenses & Credentials

Anatomic Pathology PhysicianPrimary

Pathology — Anatomic Pathology

Code: 207ZP0101X

32119(ZZ)

Research & Publications (20)

Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant.
PMID 18687426·Fertil Steril·2008
5-case
Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman.
PMID 18302251·Am J Med Genet A·2008
5-case
Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris.
PMID 17164798·Eur J Hum Genet·2007
8-other
Pre- and postnatal findings in trisomy 17 mosaicism.
PMID 16802327·Am J Med Genet A·2006
8-other
Micro-array analyses decipher exceptional complex familial chromosomal rearrangement.
PMID 16395598·Hum Genet·2006
5-case
Del(18)(q12.2q21.1) caused by a paternal sister chromatid rearrangement in a developmentally delayed girl.
PMID 15887269·Am J Med Genet A·2005
5-case
Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosettes.
PMID 15839726·PLoS Biol·2005
8-other
Somatic mosaicism for a heterozygous deletion of the survival motor neuron (SMN1) gene.
PMID 15586177·Eur J Hum Genet·2005
8-other
Order of genetic events is critical determinant of aberrations in chromosome count and structure.
PMID 15188452·Genes Chromosomes Cancer·2004
4-observational
First non-mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter --> q22.1::q22.1 --> pter) is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q- syndrome.
PMID 15103719·Am J Med Genet A·2004
5-case
Tetrasomy 21pter-->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardation.
PMID 14985397·J Med Genet·2004
5-case
A familial unbalanced subtelomeric translocation resulting in monosomy 6q27-->qter.
PMID 12676921·J Med Genet·2003
5-case
Adhesive backing foil interactions affecting the elasticity, adhesion strength of laminates, and how to interpret these properties of branded transdermal patches.
PMID 12476871·Drug Dev Ind Pharm·2002
8-other
Multicolor FISH in two and three dimensions for clastogenic analyses.
PMID 12435849·Mutagenesis·2002
6-review
Targeted inactivation of p53 in human cells does not result in aneuploidy.
PMID 11861393·Cancer Res·2002
8-other
A new strategy for the detection of subtelomeric rearrangements.
PMID 11810269·Hum Genet·2001
8-other
Live-cell microscopy of single nuclear chromosomes and genome compartments: evaluation of labeling procedure and imaging conditions.
PMID 11746090·Cytometry·2001
8-other
Additional dark G-band in the p-arm of chromosome 19 due to a paracentric inversion with a breakpoint in the pericentromeric heterochromatin.
PMID 11568924·Am J Med Genet·2001
5-case
AcroM fluorescent in situ hybridization analyses of marker chromosomes.
PMID 11511920·Hum Genet·2001
5-case
Classifying by colors: FISH-based genome analysis.
PMID 11474168·Cytogenet Cell Genet·2001
6-review

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
DEPARTMENT OF ANATOMIC PATHOLOGY, CHILDREN'S AND WOMEN', HEALTH CENTRE, 4480 OAK STREET, ROOM L220
VANCOUVER, BC 634

Location

Practice Location

DEPARTMENT OF ANATOMIC PATHOLOGY, CHILDREN'S AND WOMEN', VANCOUVER, BC
(604) 875-2395

Quick Facts

NPI
1336379437
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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