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Catherine G. Palmer
American geneticist.
Associated eponyms:
Jarcho-Levin syndrome
A syndrome of severe malformation of the spinal column and thoracic cage.
Biography:
Catherine G. Palmer was Professor of Medical Genetics, Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis. In 1981 she had the additional appointment as Assistant Dean for Graduate Studies, School of Medicine. In 1994 she retired with the title Professor Emeritus of Medical and Molecular Genetics, School of Medicine. In 2002 she was the recipient of the Distinguished Cytogeneticist Award. Palmer was recognized for her significant role in teaching as she has trained many of the currently practicing clinical cytogeneticists in the US.
Bibliography:
- Arnold J. Altman, Catherine G. Palmer, and Robert L. Baehner:
Juvenile "Chronic Granulocytic" Leukemia: A Panmyelopathy With Prominent Monocytic Involvement and Circulating Monocyte Colony-forming Cells.
Blood, 1974, 43 (3): 341-350.
- Jay L. Grosfeld, Donald S. Stepita, Walter E. Nance, and Catherine G. Palmer:
Fetus-in-Fetu: An Unusual Cause for Abdominal Mass in Infancy.
Annals of Surgery, July 1974, 180 (1): 80-84.
- Catherine G. Palmer, Charles Poland, Terry Reed and Judy Kojetin:
Partial trisomy 11,46,XX,-3,-20,+der3,+der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20.
Human Genetics, Berlin / Heidelberg, January 1976, 31 (2): 219-225.
- Elisabeth A. Keitges, Catherine G. Palmer and David D. Weaver:
Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function.
Human Genetics, December 1982, 62 (3): 210-213.
- Yongming Sun, Jack Rubinstein, Shirley Soukup, Catherine G. Palmer:
•Marker chromosome 21 identified by microdissection and FISH.
American Journal of Medical genetics, 1995, 66 (2): 151-154.
- Teresa A. Smolarek, Ruthann I. Blough, Richard S. Foster, Thomas M. Ulbright, Catherine G. Palmer, Nyla A. Heerema:
Identification of multiple chromosome 12 abnormalities in human testicular germ cell tumors by two-color fluorescence in situ hybridization (FISH).
Genes, Chromosomes and Cancer, December 1995, 14 (4): 252-258.
- Yongming Sun, Robert D. Nicholls, Merlin G. Butler, Shinji Saitoh, Bryan E. Hainline and Catherine G. Palmer:
Breakage in the SNRPN locus in a balanced 46,XY, t(15;19) Prader-Willi syndrome patient. Human Molecular Genetics, 1996, 5 (4): 517.
- Jonathan P. Park, PhD; Arthur R. Brothman, PhD; Merlin G. Butler, MD, PhD; Linda D. Cooley, MD; Gordon W. Dewald, PhD; Kurt F. Lundquist, MD; Catherine G. Palmer, MD; Shivanand R. Patil, PhD; Kathleen W. Rao, PhD; Irene A. Saikevych, MD; Nancy R. Schneider, MD, PhD; Gail H. Vance, MD; for the College of American Pathologists/American College of Medical Genetics:
Extensive Analysis of Mosaicism in a Case of Turner Syndrome. The Experience of 287 Cytogenetic Laboratories.
Archives of Pathology and Laboratory Medicine, 1999, 123 (5).381–385.
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