Authors:
Sood, R
Bonner, TI
Makalowska, I
Stephan, DA
Robbins, CM
Connors, TD
Morgenbesser, SD
Su, K
Faruque, MU
Pinkett, H
Graham, C
Baxevanis, AD
Klinger, KW
Landes, GM
Trent, JM
Carpten, JD
Citation: R. Sood et al., Cloning and characterization of 13 novel transcripts and the human RC58 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus, GENOMICS, 73(2), 2001, pp. 211-222
Authors:
Bianchi, DW
Farina, A
Weber, W
Delli-Bovi, LC
DeRiso, M
Williams, JM
Klinger, KW
Citation: Dw. Bianchi et al., Significant fetal-maternal hemorrhage after termination of pregnancy: Implications for development of fetal cell microchimerism, AM J OBST G, 184(4), 2001, pp. 703-706
Authors:
Ibraghimov-Beskrovnaya, O
Bukanov, NO
Donohue, LC
Dackowski, WR
Klinger, KW
Landes, GM
Citation: O. Ibraghimov-beskrovnaya et al., Strong homophilic interactions of the Ig-like domains of polycystin-1,the protein product of an autosomal dominant polycystic kidney disease gene, PKD1, HUM MOL GEN, 9(11), 2000, pp. 1641-1649
Authors:
Sood, R
Makalowska, I
Carpten, JD
Robbins, CM
Stephan, DA
Connors, TD
Morgenbesser, SD
Su, K
Pinkett, HW
Graham, CL
Quesenberry, MI
Baxevanis, AD
Klinger, KW
Trent, JM
Bonner, TI
Citation: R. Sood et al., The human RGL (RalGDS-like) gene: cloning, expression analysis and genomicorganization, BBA-GENE ST, 1491(1-3), 2000, pp. 285-288
Citation: Kw. Klinger et O. Ibraghimov-beskrovnaya, Polycystins - Membrane-associated proteins involved in autosomal dominant polycystic kidney disease, MEMBRANE STRUCTURE IN DISEASE AND DRUG THERAPY, 2000, pp. 409-426
Authors:
Haddow, JE
Bradley, LA
Palomaki, GE
Doherty, RA
Bernhardt, BA
Brock, DJH
Cheuvront, B
Cunningham, GC
Donnenfeld, AE
Erickson, JL
Erlick, HA
Ferrie, RM
FitzSimmons, SC
Greene, MF
Grody, WW
Haddow, PK
Harris, H
Holmes, LB
Howell, RR
Katz, M
Klinger, KW
Kloza, EM
LeFevre, ML
Little, S
Loeben, G
McGovern, M
Pyeritz, RE
Rowley, PT
Saiki, RK
Short, MP
Tabone, J
Wald, NJ
Wilker, NL
Witt, DR
Citation: Je. Haddow et al., Issues in implementing prenatal screening for cystic fibrosis: Results of a working conference (vol 1, pg 129, 1999), GENET MED, 1(5), 1999, pp. 193-193
Authors:
Haddow, JE
Bradley, LA
Palomaki, GE
Doherty, RA
Bernhardt, BA
Brock, DJH
Cheuvront, B
Cunningham, GC
Donnenfeld, AE
Erickson, JL
Erlich, HA
Ferrie, RM
FitzSimmons, SC
Greene, MF
Grody, WW
Haddow, PK
Harris, H
Holmes, LB
Howell, RR
Katz, M
Klinger, KW
Kloza, EM
LeFevre, ML
Little, S
Loeben, G
McGovern, M
Pyeritz, RE
Rowley, PT
Saiki, RK
Short, MP
Tabone, J
Wald, NJ
Wilker, NL
Witt, DR
Citation: Je. Haddow et al., Issues in implementing prenatal screening for cystic fibrosis: Results of a working conference, GENET MED, 1(4), 1999, pp. 129-135
Authors:
Watnick, T
Phakdeekitcharoen, B
Johnson, A
Gandolph, M
Wang, M
Briefel, G
Klinger, KW
Kimberling, W
Gabow, P
Germino, GG
Citation: T. Watnick et al., Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease, AM J HU GEN, 65(6), 1999, pp. 1561-1571