Holly H. Hobart

发表

Distribution of non-telomeric sites of the (TTAGGG)n telomeric sequence in vertebrate chromosomes

Robert J. Baker, Robert K. Moyzis, Oliver A. Ryder, 1990, Chromosoma.

Down-Regulation of Replication Factor C-40 (RFC40) Causes Chromosomal Missegregation in Neonatal and Hypertrophic Adult Rat Cardiac Myocytes

J. Downey, H. Ata, M. Oka, 2012, PloS one.

Bilateral semilunar valve disease in a child with partial deletion of the Williams-Beuren syndrome region is associated with elastin haploinsufficiency.

C. Morris, R. Hinton, D. Benson, 2006, The Journal of heart valve disease.

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype–phenotype analysis of five families with deletions in the Williams syndrome region

C. Mervis, C. Morris, C. Moore, 2003, American journal of medical genetics. Part A.

Blastopathies and microcephaly in a Chornobyl impacted region of Ukraine

L. Yevtushok, W. Wertelecki, Holly H. Hobart, 2014, Congenital anomalies.

Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome

C. Mervis, P. Bray-Ward, C. Morris, 2010, American journal of medical genetics. Part C, Seminars in medical genetics.

Heat shock protein 27 gene: Chromosomal and molecular location and relationship to Williams syndrome

C. Mervis, C. Morris, P. Spallone, 2003, American journal of medical genetics. Part A.

Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome

C. Mervis, P. Bray-Ward, C. Morris, 2010, PloS one.

Comparative karyology in nine-primaried oscines (Aves).

Holly H. Hobart, 1991 .

BAC-FISH refutes report of an 8p22–8p23.1 inversion or duplication in 8 patients with Kabuki syndrome

C. Morris, Holly H. Hobart, K. W. Kimberley, 2006, BMC Medical Genetics.

Inversion Common Polymorphism of the Williams Found Syndrome More Region Frequently Is a in Parents of Children With Williams Syndrome

C. Mervis, P. Bray-Ward, C. Morris, 2010 .

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

Christian R Marshall, Alexandre Reymond, Paige Kaplan, 2008, American journal of human genetics.