Citation: Ca. Wise et al., DEPARTURE FROM NEUTRALITY AT THE MITOCHONDRIAL NADH DEHYDROGENASE SUBUNIT-2 GENE IN HUMANS, BUT NOT IN CHIMPANZEES, Genetics, 148(1), 1998, pp. 409-421
Authors:
WISE CA
CLINES GA
MASSA H
TRASK BJ
LOVETT M
Citation: Ca. Wise et al., IDENTIFICATION AND LOCALIZATION OF THE GENE FOR EXTL, A 3RD MEMBER OFTHE MULTIPLE EXOSTOSES GENE FAMILY, PCR methods and applications, 7(1), 1997, pp. 10-16
Citation: Ca. Wise et al., COMPARATIVE NUCLEAR AND MITOCHONDRIAL GENOME DIVERSITY IN HUMANS AND CHIMPANZEES, Molecular biology and evolution, 14(7), 1997, pp. 707-716
Authors:
WISE CA
CHIANG LC
PAZNEKAS WA
SHARMA M
MUSY MM
ASHLEY JA
LOVETT M
JABS EW
Citation: Ca. Wise et al., TCOF1 GENE ENCODES A PUTATIVE NUCLEOLAR PHOSPHOPROTEIN THAT EXHIBITS MUTATIONS IN TREACHER-COLLINS-SYNDROME THROUGHOUT ITS CODING REGION, Proceedings of the National Academy of Sciences of the United Statesof America, 94(7), 1997, pp. 3110-3115
Authors:
WISE CA
GALLARDO TD
SIMMONS A
MUSY M
ASHLEY JA
LOVETT M
Citation: Ca. Wise et al., IDENTIFICATION OF NOVEL GENES FROM CHROMOSOME 5-SPECIFIC CDNA LIBRARIES, American journal of human genetics, 61(4), 1997, pp. 189-189
Authors:
DELMASTRO RG
ASHLEY JA
CLINES GA
SIMMONS AD
WISE CA
LOVETT M
Citation: Rg. Delmastro et al., RAPID CONSTRUCTION OF TRANSCRIPTION MAPS BY HYBRIDIZATION OF YACS TO CHROMOSOME-SPECIFIC CDNA LIBRARIES, American journal of human genetics, 57(4), 1995, pp. 1499-1499
Authors:
WISE CA
ASHLEY JA
GALLARDO TD
DELMASTRO R
LI X
JABS EW
LOVETT M
Citation: Ca. Wise et al., TRANSCRIPTION MAPPING OF THE LEGION CONTAINING THE LOCUS FOR TREACHER-COLLINS SYNDROME, American journal of human genetics, 57(4), 1995, pp. 1589-1589
Citation: Ca. Wise et al., CMTIA DUPLICATION ANALYSIS IN THE DIAGNOSTIC EVALUATION OF PATIENTS WITH PERIPHERAL NEUROPATHY - REPLY, American journal of human genetics, 54(4), 1994, pp. 728-729
Authors:
ROA BB
GARCIA CA
SUTER U
KULPA DA
WISE CA
MUELLER J
WELCHER AA
SNIPES GJ
SHOOTER EM
PATEL PI
LUPSKI JR
Citation: Bb. Roa et al., CHARCOT-MARIE-TOOTH DISEASE TYPE-1A - ASSOCIATION WITH A SPONTANEOUS POINT MUTATION IN THE PMP22 GENE, The New England journal of medicine, 329(2), 1993, pp. 96-101
Authors:
WISE CA
GARCIA CA
DAVIS SN
ZHANG HJ
LIU PT
PATEL PI
LUPSKI JR
Citation: Ca. Wise et al., MOLECULAR ANALYSES OF UNRELATED CHARCOT-MARIE-TOOTH (CMT) DISEASE PATIENTS SUGGEST A HIGH-FREQUENCY OF THE CMT-IA DUPLICATION, American journal of human genetics, 53(4), 1993, pp. 853-863
Authors:
WISE CA
LI X
GRIFFIN C
HAWKINS A
LOVETT M
JABS EW
Citation: Ca. Wise et al., A 3MB YAC CONTIG FROM CHROMOSOME-5 COVERING GRL TO SPARC AND INCLUDING THE TREACHER-COLLINS SYNDROME LOCUS, American journal of human genetics, 53(3), 1993, pp. 1373-1373