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LAURA ROOMS, MD

MD

Pediatric Hematology & Oncology Physician

NPI: 1689642910Individual

Specialties, Licenses & Credentials

Pediatric Hematology & Oncology PhysicianPrimary

Pediatrics — Pediatric Hematology-Oncology

Code: 2080P0207X

20770(OK)

Research & Publications (13)

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis.
PMID 18178631·J Med Genet·2008
5-case
Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches.
PMID 18159213·Eur J Hum Genet·2008
8-other
A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
PMID 17786114·Clin Dysmorphol·2007
5-case
Dandy-Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33).
PMID 17431901·Am J Med Genet A·2007
5-case
Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation.
PMID 16991117·Hum Mutat·2007
8-other
TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.
PMID 16773126·Eur J Hum Genet·2006
7-preclinical
Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics.
PMID 16451137·Clin Genet·2006
5-case
A subterminal deletion of the long arm of chromosome 10: a clinical report and review.
PMID 16419133·Am J Med Genet A·2006
5-case
Subtelomeric rearrangements in the mentally retarded: a comparison of detection methods.
PMID 15880643·Hum Mutat·2005
4-observational
Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype.
PMID 15822126·Am J Med Genet A·2005
5-case
Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA).
PMID 14695528·Hum Mutat·2004
8-other
Hemophagocytic lymphohistiocytosis masquerading as child abuse: presentation of three cases and review of central nervous system findings in hemophagocytic lymphohistiocytosis.
PMID 12728123·Pediatrics·2003
5-case

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

Contact & Hours

Address
1200 N PHILLIPS AVE, SUITE 10000
OKLAHOMA CITY, OK 73104

Location

Practice Location

1200 N PHILLIPS AVE, OKLAHOMA CITY, OK
(405) 271-4412

Quick Facts

NPI
1689642910
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
13

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