Carol Booth - Concepedia

Author

Carol Booth

Advocate Lutheran General Hospital

Also Known As

C Booth, C. Booth, C.C. Booth, CAROL BOOTH, Carol Booth

Publications

Citations

H-Index

Concepts

All Affiliations

Advocate Lutheran General Hospital Baylor College of Medicine University of Chicago

About

Carol Booth is an author at Advocate Lutheran General Hospital specializing in pediatrics, medicine, and obstetrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	298
2	Anatomy	1	1	22
3	Gastroenterology	1	1	23
4	Molecular Medicine	1	1	276
5	Obstetrics	1	1	22

Carol Booth

Publications

620

Citations

H-Index

Page 1

	Year	Citations
Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations Jennifer J. Johnston, Isabelle Olivos‐Glander, Christina Killoran, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsGenetic Epidemiology	2005	276
A loss of function mutation in the <i>COL9A2</i> gene causes autosomal recessive Stickler syndrome Stuart G. Baker, Carol Booth, Corrine Fillman, American Journal of Medical Genetics Part A	2011	107
Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism C. E. Jones, Carol Booth, Debra Rita, Prenatal Diagnosis	1995	98
A second-site mutation at phenylalanine-137 that increases catalytic efficiency in the mutant aspartate-27 .fwdarw. serine Escherichia coli dihydrofolate reductase Elizabeth E. Howell, Carol Booth, Martin F. Farnum, Biochemistry	1990	29
Acute myeloid leukemia and myelodysplasia following intensive chemotherapy for breast cancer. S Roman-Unfer, Bitran Jd, Stephen B. Hanauer, PubMed	1995	29
Familial occurrence of congenital colonic atresia Raghbir Benawra, Bhagya L. Puppala, Henry H. Mangurten, The Journal of Pediatrics Developmental AnomalyGenetic DisorderCongenital Colonic AtresiaGastroenterologyPediatric Gastroenterology	1981	23
Prenatal diagnosis of Weyers syndrome (deficient ulnar and fibular rays with bilateral hydronephrosis) B. Rafael Elejalde, Maria Mercedes de Elejalde, Carol Booth, American Journal of Medical Genetics Developmental AnomalyDeficient UlnarMedicineFetal MedicinePediatrics	1985	22
Ethnic heterogeneity and cystic fibrosis transmembrane regulator (CFTR) mutation frequencies in Chicago-area CF families. Carole Ober, Laura Lester, C Mott, PubMed	1992	18
Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysis Alice Martin, Hope Northrup, David H. Ledbetter, American Journal of Medical Genetics	1988	18

Page 1