Mary C. Phelan - Concepedia

Author

Mary C. Phelan

Also Known As

M C Phelan, M Phelan, M. C. Phelan, M. Phelan, M.C. Phelan, MARY C. PHELAN, Mary C Phelan, Mary C. Phelan, Mary Catherine Phelan, Mary Phelan

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Greenwood Genetic Center Roche (Switzerland)Molecular Pathology Laboratory Network (United States)Roche (United Kingdom)Self Regional Healthcare

About

Mary C. Phelan is an author at Greenwood Genetic Center specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	24	1.6K
2	Engineering	4	4	141
3	Public Health	2	2	170
4	Health Sciences	1	1	86
5	Social Sciences	1	1	45

Mary C. Phelan

Publications

Citations

H-Index

Page 1

	Year	Citations
Autism and maternally derived aberrations of chromosome 15q Richard J. Schroer, Mary C. Phelan, Ron C. Michaelis, American Journal of Medical Genetics	1998	372
22q13 deletion syndrome Mary C. Phelan, R. Curtis Rogers, Robert A. Saul, American Journal of Medical Genetics	2001	274
Vascular Steal: The Pathogenetic Mechanism Producing Sirenomelia and Associated Defects of the Viscera and Soft Tissues Roger E. Stevenson, Kenneth Lyons Jones, Mary C. Phelan, PEDIATRICS BiologyVitelline Artery ComplexVascular StealDevelopmental BiologyAssociated Defects	1986	254
Deletion 22q13.3 syndrome Mary C. Phelan Orphanet Journal of Rare Diseases Down SyndromeDevelopmental AnomalyGene Deletion DataDevelopmental BiologyMendelian Disorder	2008	222
Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities Evelin Schröck, Timothy Veldman, Hesed Padilla‐Nash, Human Genetics Karyotype ImagingChromatinSpectral KaryotypingCytogeneticsGenetics	1997	177
Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome. Allyn McConkie‐Rosell, Ave M. Lachiewicz, Gail A. Spiridigliozzi, PubMed	1993	169
Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals Mary C. Phelan, R. Curtis Rogers, Kate B. Clarkson, American Journal of Medical Genetics	1995	132
Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf–Hirschhorn syndrome James F. Gusella, Rudolph E. Tanzi, Patricia I. Bader, Nature Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyPathology	1985	128
Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop Mary C. Phelan, Roger E. Stevenson, E. Vernon Anderson American Journal of Medical Genetics	1993	90
Discordant Expression of Fetal Hydantoin Syndrome in Heteropaternal Dizygotic Twins Mary C. Phelan, John M. Pellock, Walter E. Nance New England Journal of Medicine GeneticsMolecular GeneticsEpigeneticsFetal Hydantoin SyndromeEmbryology	1982	89

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