HollyH.HobartMD

Medical Genetics • Las Vegas, NV

Clinical Cytogenetics, Ph.D. Medical Genetics

Physician

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Office
1707 W. Charleston Blvd- Dba Nevada Genetics Laboratory
110-B
Las Vegas, NV 89102
Phone+1 702-671-5055

Fax+1 702-671-0193
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Summary

Dr. Holly Hobart, MD is a board certified medical geneticist in Las Vegas, Nevada.

Certifications & Licensure

American Board of Medical Genetics and Genomics Clinical Cytogenetics and Genomics

Publications & Presentations

PubMed

13 citations
Blastopathies and microcephaly in a Chornobyl impacted region of Ukraine
Wladimir Wertelecki, Lyubov Yevtushok, Natalia Zymak-Zakutnia, Bin Wang, Zoriana Sosyniuk, Serhiy Lapchenko, Holly H Hobart> ;Congenital Anomalies. 2014 Aug 1
3 citations
Down-Regulation of Replication Factor C-40 (RFC40) Causes Chromosomal Missegregation in Neonatal and Hypertrophic Adult Rat Cardiac Myocytes
Hirotaka Ata, Deepa Shrestha, Masahiko Oka, Rikuo Ochi, Chian Ju Jong, Sarah A. Gebb, John T. Benjamin, Stephen W. Schaffer, Holly H. Hobart, James M. Downey, Ivan F. ...> ;Plos One. 2012 Jun 14
12 citations
Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.
Ariel M. Pani, Holly H. Hobart, Colleen A. Morris, Carolyn B. Mervis, Patricia Bray-Ward, Kendra W. Kimberley, Cecilia M. Rios, Robin C. Clark, Maricela D. Gulbronson,...> ;Plos One. 2010 Aug 31
32 citations
Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome.
Holly H. Hobart, Colleen A. Morris, Carolyn B. Mervis, Ariel M. Pani, Doris J. Kistler, Cecilia M. Rios, Kendra W. Kimberley, Ronald G. Gregg, Patricia Bray-Ward> ;American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2010 May 15
13 citations
BAC-FISH refutes report of an 8p22–8p23.1 inversion or duplication in 8 patients with Kabuki syndrome
Kendra W. Kimberley, Colleen A. Morris, Holly H. Hobart> ;BMC Medical Genetics. 2006 May 18
7 citations
Bilateral semilunar valve disease in a child with partial deletion of the Williams-Beuren syndrome region is associated with elastin haploinsufficiency.
Robert B. Hinton, Gail H. Deutsch, Jeffrey M. Pearl, Holly H. Hobart, Colleen A. Morris, D. Woodrow Benson> ;The Journal of Heart Valve Disease. 2006 May 1
3 citations
Unrelated patients with a rearrangement of chromosome 2 causing duplication of 2p23 and deletion of 2q37
Linlea Armstrong, Judith Allanson, David D. Weaver, Carole J. Bevan, Holly H. Hobart> ;American Journal of Medical Genetics. Part A. 2005 Apr 30
120 citations
GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.
Colleen A. Morris, Carolyn B. Mervis, Holly H. Hobart, Ronald G. Gregg, Jacquelyn Bertrand, Gregory J. Ensing, Annemarie Sommer, Cynthia A. Moore, Robert J. Hopkin, Pa...> ;American Journal of Medical Genetics. Part A. 2003 Nov 15
24 citations
Heat shock protein 27 gene: chromosomal and molecular location and relationship to Williams syndrome.
A. Dean Stock, Patricia A. Spallone, Thomas R Dennis, Dale Netski, Colleen A. Morris, Carolyn B. Mervis, Holly H. Hobart> ;American Journal of Medical Genetics. Part A. 2003 Jul 30
443 citations
Distribution of non-telomeric sites of the (TTAGGG)n telomeric sequence in vertebrate chromosomes.
Julianne Meyne, Robert J. Baker, Holly H. Hobart, T. C. Hsu, Oliver A. Ryder, Oscar G. Ward, John E. Wiley, Doris H. Wurster-Hill, Terry L. Yates, Robert K. Moyzis> ;Chromosoma. 1990 Apr 1
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