Deep Blue: Browsing Human Genetics, Department of by Title

Mouse chromosome 3

Todd, John A.; Seldin, Michael F.; Prins, Jan-Bas; Rodrigues, Nanda R.; Meisler, Miriam H. (Springer-Verlag, 1993-01)

(799KB)

Mouse Chromosome 3

Wakeland, Edward K.; Seldin, Michael F.; Rodrigues, Nanda R.; Todd, John A.; Meisler, Miriam H. (Springer-Verlag, 1992-01)

(949.3KB)

Mouse chromosome 3

Meisler, Miriam H. (Springer-Verlag; Springer-Verlag New York Inc., 1991-03)

(787.3KB)

Multicolor FISH Mapping of YAC Clones in 3p14 and Identification of a YAC Spanning both FRA3B and the t(3;8) Associated with Hereditary Renal Cell Carcinoma

Wilke, Charles M.; Guo, Sun-Wei; Hall, Bryan K.; Boldog, Ferenc; Gemmill, Robert M.; Chandrasekharappa, Settara C.; Barcroft, Christine L.; Drabkin, Harry A.; Glover, Thomas W. (Elsevier, 1994-07-15)

(551.6KB)

Multicolor FISH Mapping with Alu-PCR-Amplified YAC Clone DNA Determines the Order of Markers in the BRCA1 Region on Chromosome 17q12-q21

Flejter, Wendy L.; Barcroft, Christine L.; Guo, Sun-Wei; Lynch, Eric D.; Boehnke, Michael; Chandrasekharappa, Settara C.; Hayes, Steve T.; Collins, Francis S.; Weber, Barbara L.; Glover, Thomas W. (Elsevier, 1993-09)

(569KB)

Multiple forms of genetic instability within a 2-Mb chromosomal segment of 3q26.3–q27 are associated with development of esophageal adenocarcinoma

Lin, Lin; Wang, Zhuwen; Prescott, Michael S.; van Dekken, Herman; Thomas, Dafydd G.; Giordano, Thomas J.; Chang, Andrew C.; Orringer, Mark B.; Gruber, Stephen B.; Moran, John V.; Glover, Thomas W.; Beer, David G. (Wiley Subscription Services, Inc., A Wiley Company, 2006-04)

(811KB)

Mutants of chinese hamster cells deficient in thymidylate synthetase

Li, I-Chian; Chu, Ernest H. Y. (Wiley Subscription Services, Inc., A Wiley Company, 1984-08)

(740.1KB)

Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing Communicated by Peter Byers

Otto, Edgar A.; Helou, Juliana; Allen, Susan J.; O'Toole, John F.; Wise, Eric L.; Ashraf, Shazia; Attanasio, Massimo; Zhou, Weibin; Wolf, Matthias T. F.; Hildebrandt, Friedhelm (Wiley Subscription Services, Inc., A Wiley Company, 2008-03)

(330.4KB)

Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J

Chow, Clement Y.; Zhang, Yanling; Dowling, James J.; Jin, Natsuko; Adamska, Maja; Shiga, Kensuke; Szigeti, Kinga; Shy, Michael E.; Li, Jun; Zhang, Xuebao; Lupski, James R.; Weisman, Lois S.; Meisler, Miriam H. (Nature Publishing Group, 2007-07-05)

(892.8KB)

MUTATION SYSTEMS IN CULTURED MAMMALIAN CELLS *

Chu, Ernest H. Y. (Blackwell Publishing Ltd, 1983-06)

(623.8KB)

Mutation Watch

Meisler, Miriam H. (Springer-Verlag; Springer-Verlag New York Inc., 1997-05)

(27.8KB)

Mutation watch: Mouse brachyury ( T ), the T-box gene family, and human disease

Meisler, Miriam H. (Springer-Verlag; Springer-Verlag New York Inc., 1997-11)

(20.5KB)

Mutation watch:PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafness

Meisler, Miriam H. (Springer-Verlag; Springer-Verlag New York Inc., 1997-08)

(28.3KB)

Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis Communicated by JÜrgen Horst Online Citation: Human Mutation , Mutation in Brief #797 (2005) Online http://www3.interscience.wiley.com/homepages/38515/pdf/797.pdf

Hoefele, Julia; Sudbrak, Ralf; Reinhardt, Richard; Lehrack, Silvia; Hennig, Steffen; Imm, Anita; Muerb, Ulla; Utsch, Boris; Attanasio, Massimo; O'Toole, John F.; Otto, Edgar A.; Hildebrandt, Friedhelm (Wiley Subscription Services, Inc., A Wiley Company, 2005-04)

(131.6KB)

Mutations of phage P22 affecting phage DNA synthesis and lysogenization

Levine, Myron; Schott, Carol (Elsevier, 1971-11-28)

(859.9KB)

Nestin-Cre mediated deletion of Pitx2 in the mouse This article is a US Government work and, as such, is in the public domain in the United States of America.

Sclafani, Anthony M.; Skidmore, Jennifer M.; Ramaprakash, Hemanth; Trumpp, Andreas; Gage, Philip J.; Martin, Donna M. (Wiley Subscription Services, Inc., A Wiley Company, 2006-07)

(2.6MB)

NF1-related locus on chromosome 15

Legius, Eric; Marchuk, Douglas A.; Hall, Bryan K.; Andersen, Lone B.; Wallace, Margaret R.; Collins, Francis S.; Glover, Thomas W. (Elsevier, 1992-08)

(431.7KB)

No association between DFNA6 and Pro250Arg mutation in FGFR3

Bespalova, Irina N.; Burmeister, Margit L.; Lesperance, Marci M. (John Wiley & Sons, Inc., 1999-10-15)

(39.8KB)

No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations

Wiggins, Roger C.; Mucha, Bettina E.; Fuchshuber, Arno; Lichtenberger, Anne; Hildebrandt, Friedhelm; Ruf, Rainer G.; Schultheiss, Michael (Springer-Verlag; IPNA, 2004-12)

(155KB)

A novel VEGFR3 mutation causes Milroy disease How to cite this article: Butler MG, Dagenais SL, Rockson SG, Glover TW. 2007. A novel VEGFR3 mutation causes Milroy disease. Am J Med Genet Part A 143A:1212–1217.

Butler, Matthew Gregory; Dagenais, Susan L.; Rockson, Stanley G.; Glover, Thomas W. (Wiley Subscription Services, Inc., A Wiley Company, 2007-06-01)

(272.8KB)

A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies How to cite this article: Jensen DR, Martin DM, Gebarski S, Sahoo T, Brundage EK, Chinault AC, Otto EA, Chaki M, Hildebrandt F, Cheung SW, Lesperance MM. 2009. A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies. Am J Med Genet Part A 149A:396–402.

Jensen, Daniel R.; Martin, Donna M.; Gebarski, Stephen S.; Sahoo, Trilochan; Brundage, Ellen K.; Chinault, A. Craig; Otto, Edgar A.; Chaki, Moumita; Hildebrandt, Friedhelm; Cheung, Sau Wai; Lesperance, Marci M. (Wiley Subscription Services, Inc., A Wiley Company, 2009-03)

(283.2KB)

Novel cystatin B mutation and diagnostic PCR assay in an unverricht-lundborg progressive myoclonus epilepsy patient

Bespalova, Irina N.; Adkins, Steve; Pranzatelli, Michael R.; Burmeister, Margit L. (Wiley Subscription Services, Inc., A Wiley Company, 1997-09-19)

(198.4KB)

Novel inhibition of carbonic anhydrase isozymes I, II and III by carbamoyl phosphate

Carter, Nicholas D.; Chegwidden, W. Richard; Hewett-Emmett, David; Jeffery, S.; Shiels, A.; Tashian, Richard E. (Elsevier, 1984-01-09)

(431.3KB)

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change

Hiriyanna, Kelaginamane T.; Bingham, Eve L.; Yashar, Beverly M.; Ayyagari, Radha; Fishman, Gerald A.; Small, Kent W.; Weinberg, David V.; Weleber, Richard G.; Lewis, Richard A.; Andreasson, Sten; Richards, Julia E.; Sieving, Paul A. (John Wiley & Sons, Inc., 1999-11)

(192.4KB)

Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes

Keegan, Catherine E.; Hutz, Janna E.; Krause, Andrea S.; Koehler, Katrin; Metherell, Louise A.; Boikos, Sosipatros; Stergiopoulos, Sotirios; Clark, Adrian J. L.; Stratakis, Constantine A.; Huebner, Angela; Hammer, Gary D. (Blackwell Publishing Ltd, 2007-08)

(117.2KB)