A microsatellite-based index map of human chromosome 11 (English)
- New search for: Litt, M.
- New search for: Kramer, P.
- New search for: Hauge, X.Y.
- New search for: Weber, J.L.
- New search for: Wang, Z.
- New search for: Wilkle, P.J.
- New search for: Holt, M.S.
- New search for: Mishra, S.
- New search for: Donis-Keller, H.
- New search for: Warnich, L.
- New search for: Retief, A.E.
- New search for: Jones, C.
- New search for: Welssenbach, J.
- New search for: Litt, M.
- New search for: Kramer, P.
- New search for: Hauge, X.Y.
- New search for: Weber, J.L.
- New search for: Wang, Z.
- New search for: Wilkle, P.J.
- New search for: Holt, M.S.
- New search for: Mishra, S.
- New search for: Donis-Keller, H.
- New search for: Warnich, L.
- New search for: Retief, A.E.
- New search for: Jones, C.
- New search for: Welssenbach, J.
In:
Human molecular genetics
;
2
, 7
;
909-
;
1993
- Article (Journal) / Electronic Resource
-
Title:A microsatellite-based index map of human chromosome 11
-
Contributors:Litt, M. ( author ) / Kramer, P. ( author ) / Hauge, X.Y. ( author ) / Weber, J.L. ( author ) / Wang, Z. ( author ) / Wilkle, P.J. ( author ) / Holt, M.S. ( author ) / Mishra, S. ( author ) / Donis-Keller, H. ( author ) / Warnich, L. ( author )
-
Published in:Human molecular genetics ; 2, 7 ; 909-
-
Publisher:
- New search for: Oxford University Press
-
Publication date:1993-07-01
-
ISSN:
-
DOI:
-
Type of media:Article (Journal)
-
Type of material:Electronic Resource
-
Language:English
-
Source:
Table of contents – Volume 2, Issue 7
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 847
-
Positional cloning uncovers a new old oncogeneFrischauf, Anna-Maria et al. | 1993
- 849
-
Malignant hyperthermia hots up!Johnson, Keith et al. | 1993
- 851
-
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTCDonis-Keller, Helen / Dou, Shenshen / Chi, David / Carlson, Katrin M. / Toshima, Koji / Lairmore, Terry C. / Howe, James R. / Moley, Jeffrey F. / Goodfellow, Paul / Wells, Samuel A. et al. | 1993
- 857
-
Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the {alpha}1, {beta}1, and {gamma} subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defectSudbrak, R. / Golla, A. / Hogan, K. / Powers, P. / Gregg, R. / Chesne, I.Du / Lehmann-Horn, F. / Deufel, T. et al. | 1993
- 863
-
Genetic mapping of the {beta}1- and {gamma}-subunits of the human skeletal muscle L-type voltage-dependent calcium channel on chromosome 17q and exclusion as candidate genes for malignant hyperthermia susceptibilitylles, David E. / Segers, Bart / Sengers, Robert C.A. / Monsieurs, Koen / Heytens, Luc / Halsall, P.Jane / Hopkins, Philip M. / Ellis, F.Richard / Hall-Curran, Julle L. / Stewart, Alistair D. et al. | 1993
- 869
-
Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7Olson, Timothy M. / Michels, Virginia V. / Lindor, Noralane M. / Pastores, Gregory M. / Weber, JamesL. / Schaid, DanielJ. / Driscoll, David J. / Feldt, Robert H. / Thibodeau, Stephen N. et al. | 1993
- 875
-
Exclusion of the involvement of all known Retinitis Pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8)Kumar-Singh, Rajendra / Farrar, G.Jane / Mansergh, Fiona / Kenna, Paul / Bhattacharya, Shoml / Gal, Andreas / Humphries, Peter et al. | 1993
- 879
-
Mapping the Von Hippel -- Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresisRichards, Frances M. / Phipps, Maude E. / Latlf, Farida / Yao, Masahlro / Crossey, Paul A. / Foster, Kelth / Llnehan, W. Marston / Affara, Nabeel A. / Lerman, Michael I. / Zbar, Berton et al. | 1993
- 883
-
Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XISTLepplg, Kathleen A. / Brown, Carolyn J. / Bressler, Steven L. / Gustashaw, Karen / Pagon, Roberta A. / Willard, Huntington F. / Disteche, Christine M. et al. | 1993
- 889
-
Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of human chromosome 4Zuo, Jlan / Robblns, Carolyn / Bahariloo, Slamak / Cox, David R. / Myers, Richard M. et al. | 1993
- 901
-
A transcription map of the region containing the Huntington disease geneRommens, J.M. / Lin, B. / Hutchinson, G.B. / Andrew, S.E. / Goldberg, Y.P. / Glaves, M.L. / Graham, R. / Lal, V. / McArthur, J. / Nasir, J. et al. | 1993
- 909
-
A microsatellite-based index map of human chromosome 11Litt, M. / Kramer, P. / Hauge, X.Y. / Weber, J.L. / Wang, Z. / Wilkle, P.J. / Holt, M.S. / Mishra, S. / Donis-Keller, H. / Warnich, L. et al. | 1993
- 915
-
PAX6 mutations in aniridiaM.Hanson, Isabel / Seawright, Anne / Hardman, Karen / Hodgson, Shirley / Zaletayev, Dmitri / Fekete, Gyorgy / Heyningen, Veronica van et al. | 1993
- 921
-
Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patientGreger, Valerie / Woolf, Elizabeth / Lalande, Marc et al. | 1993
- 925
-
Identical APC exon 15 mutations result in a variable phenotype in familial adenomatous polyposisPaul, Philip / Letteboer, Tom / Gelbert, Larry / Groden, Joanna / White, Ray / Coppes, Max J. et al. | 1993
- 933
-
Molecular definition of the extreme size polymorphism in apolipoprotein(a)Lackner, Carolin / Cohen, Jonathan C. / Hobbs, Helen H. et al. | 1993
- 941
-
Characterization of the human fumarylacetoacetate hydrolase gene and identification of a missense mutation abolishing enzymatic activityLabelle, Yves / Phaneuf, Daniel / Leclerc, Barbara / M.Tanguay, Robert et al. | 1993
- 947
-
The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regionsWapenaar, Martin C. / Bassl, Maria T. / Schaefer, Laura / Grillo, Alessandra / Ferrero, Giovanni B. / Chlnault, A.Craig / Ballabio, Andrea / Zoghbi, Huda Y. et al. | 1993
- 953
-
Discordant phenotype of two overlapping deletions involving the PAX3 gene in chromosome 2q35Pasterls, N.German / J.Trask, Barbara / Sheldon, Susan / L.Gorskl, Jerome et al. | 1993
- 961
-
Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndromePereira, Lygia / D'Alessio, Marina / Ramirez, Francesco / R.Lynch, Jennifer / Sykes, Bryan / Pangilinan, Theresa / Bonadio, Jeffrey et al. | 1993
- 969
-
Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23M.McConville, Carmel / J.Byrd, Philip / J.Ambrose, Helen / Stankovic, Tanja / Ziv, Yael / Bar-Shira, Anat / Vanagaite, Lina / Rotman, Galit / Shiloh, Yosef / T.Gillett, Godfrey et al. | 1993
- 975
-
Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencingBlanquet, Véronique / Turleau, Catherine / Gross, Marie-Sylvie / Goossens, Michel / Besmond, Claude et al. | 1993
- 981
-
Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangementsUpadhyaya, M. / Jardine, P. / Maynard, J. / Farnham, J. / Sarfarazi, M. / Wijmenga, C. / Hewitt, J.E. / Frants, R. / Harper, P.S. / Lunt, P.W. et al. | 1993
- 989
-
An alternatively-spliced mRNA in the carboxy terminus of the neurofibromatosis type 1 (NF1) gene is expressed in muscleH.Gutmann, David / B.Andersen, Lone / L.Cole, Jeffery / Swaroop, Manju / S.Collins, Francis et al. | 1993
- 993
-
The state of DNA methylation in the promoter and exon 1 regions of the human gene for the interleukin-2 receptor {alpha} chain (IL-2R{alpha}) in various cell typesBehn-Krappa, Annett / Doerfler, Walter et al. | 1993
- 1001
-
Characterization of a human {alpha}1-antitrypsin null allele involving aberrant mRNA splicingE.Laubach, Victor / Ryan, W.John / Brantly, Mark et al. | 1993
- 1007
-
Haplotype analysis to determine the position of a mutation among closely linked DNA markersRamsay, Michele / Williamson, Robert / Estivill, Xavier / Wainwright, Brandon J. / Ho, Meng-Falt / Halford, Stephanie / Kere, Juha / Savilahti, Erkki / Chapelle, Albert de la / Schwartz, Marianne et al. | 1993
- 1015
-
Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracersMorral, Núria / Nunes, Virginia / Casals, Teresa / Chillón, Miguel / Giménez, Javier / Bertranpetit, Jaume / Estivill, Xavier et al. | 1993
- 1023
-
Variation of short tandem repeats within and between populationsJ.Wall, Wilson / Williamson, Robert / Petrou, Mary / Papaioannou, Dla / H.Parkin, Brian et al. | 1993
- 1031
-
Functional complementation in mouse -- human radiation hybrids assigns the putative murine scid gene to the pericentric region of human chromosome 8Komatsu, Kenshi / Ohta, Tohru / Jinno, Yoshihiro / Nlikawa, Norio / Okumura, Yutaka et al. | 1993
- 1035
-
A physical map of the C6 and C7 complement component gene region on chromosome 5p13Hobart, M.J. / Fernie, B.A. / DiSciplo, R.G. / Lachmann, P.J. et al. | 1993
- 1037
-
Non-conservation of a catalytic residue in a dipeptidyl aminopeptidase IV-related protein encoded by a gene on human chromosome 7Yokotani, Noboru / Doi, Katsuml / J.Wenthold, Robert / Wada, Kelji et al. | 1993
- 1041
-
An exonic point mutation creates a MaeIll site in the androgen receptor gene of a family with complete androgen insensitivity syndromeLobaccaro, Jean-Marc / Lumbroso, Serge / Ktari, Rafiaa / Dumas, Robert / Sultan, Charles et al. | 1993
- 1045
-
Sequencing of exons 16 and 17 of the {beta}-amyloid precursor protein gene fails to identify new mutations in Swedish Alzheimer's disease patientsJohnston, Janet / Lillus, Lena / Axelman, Karin / Cowburn, Richard / Johansson, Kurt / Vlltanen, Matti / Winblad, Bengt / Lannfelt, Lars et al. | 1993
- 1047
-
A dinucleotide deletion (-{Delta}GA115) in the tyrosinase gene responsible for type I-A (tyrosinase negative) oculocutaneous albinism in a Pakistani individualS.Oetting, William / P.Fryer, James / A.King, Richard et al. | 1993
- 1049
-
A 4 basepair deletion in exon 4 of the human lipoprotein lipase gene results in type I hyperlipoproteinemiaMa, Yuanhong / Liu, Ming-Sun / Zhang, Hanfang / J.Forsythe, Ian / D.Brunzell, John / R.Hayden, Michael et al. | 1993
- 1051
-
Mutation analysis in patients with the typical form of Anderson -- Fabry diseaseDavies, Joanna P. / Winchester, Bryan G. / Malcolm, Sue et al. | 1993
- 1055
-
A missense mutation (178Cys{uparrow}Tyr) and two neutral dimorphisms (115His and 333Ser) in the human coagulation factor VII geneMarchetti, G. / Ferrati, M. / Patracchini, P. / Redaelli, R. / Bernardi, F. et al. | 1993
- 1057
-
A new disease-causing mutation in the GAP-related domain of the NF1 geneAnglani, F. / Murgla, A. / Bedln, S. / Bresin, E. / Bernardl, F. / Clementi, M. / Tenconi, R. et al. | 1993
- 1061
-
A novel missense mutation in the phenylalanine hydroxylase gene of a homozygous Pakistani patient with non-PKU hyperphenylalaninemiaGuldberg, Per / C.Lou, Hans / Henriksen, Karen Frils / Mlkkelsen, Ingrld / Olsen, Blrgltte / Hoick, Birgit / Guttler, Flemmlng et al. | 1993
- 1063
-
An 8-bp deletion in exon B of the iduronate-2-sulphatase gene in a case of Hunter diseaseGoldenfum, Sandra / Malcolm, Sue / Winchester, Bryan et al. | 1993
- 1067
-
A novel nonsense mutation, W846XI (amber termination), in exon 14a of the cystic fibrosis transmembrane conductance regulator (CFTR) geneCheadle, Jeremy P. / Al-Jader, Layla N. / Meredith, Allson L. et al. | 1993
- 1069
-
Human erythropoietic protoporphyria: identification of a mutation at the splice donor site of intron 7 causing exon 7 skipping of the ferrochelatase geneNakahashi, Yoshitsugu / Miyazaki, Hiroaki / Kadota, Yoichi / Naitoh, Yuji / Inoue, Kyoichi / Yamamoto, Masayuki / Hayashi, Norio / Taketani, Shigeru et al. | 1993
- 1071
-
Identification of three rare frameshift mutations in exon 13 of the cystic fibrosis gene: 1918delGC, 2118del4 and 2372del8Chevalier-Porst, F. / Mathieu, M. / Bozon, D. et al. | 1993
- 1073
-
A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 geneIgarashi, Yutaka / Ogawa, Masamichi / Kamijo, Takashi / Iwatani, Noritaka / Nishi, Yoshikazu / Kohno, Hitoshi / Masumura, Takehiro / Koga, Junichi et al. | 1993
- 1075
-
A new mutation of exon 5 of the P53 gene in breast cancerCarrere, N. / Leblanc, R.M. / Begueret, J. / Blouin, P. / Cheyrou, A. et al. | 1993
- 1077
-
Dinucleotide repeat polymorphisms at the D4S126 and D4S114 lociTagle, Danilo A. / Blanchard-McQuate, Kristina L. / Valdes, John / Castilla, Lucio / Collins, Francis S. et al. | 1993
- 1078
-
Dinucleotide repeat polymorphism at the DXS1146 locusHong, Hee-Kyung / Giorda, Roberto / Trucco, Massimo / Chakravarti, Aravinda et al. | 1993
- 1079
-
The detection of a VNTR at the Huntington disease genetic marker D4S10Cariock, Leon / Vo, Trieu et al. | 1993
- 1079a
-
A TaqI site identifies the *A allele at the ACP1 locusSensabaugh, GF / Lazaruk, KA et al. | 1993
- 1079-a
-
A Taql site identifies the *A allele at the ACP1 locusSensabaugh, G.F. / Lazaruk, K.Ayer et al. | 1993
- 1080
-
Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12-q22Flejter, Wendy L. / Kukowska-Latallo, Jolanta F. / Kiousis, Sam / Chandrasekharappa, Settara C. / King, Stephanie E. / Chamberlain, Jeffrey S. et al. | 1993
- 1080-a
-
Human Bg/ll/Bc/l RFLP recognized by 3' region of human MAP 2 gene probeDing, Yuan / Reed, Danielle R. / Price, R.Arlen et al. | 1993
- 1080a
-
Human BglII/BclI RFLP recognized by 3' region of human MAP 2 gene probeDing, Y / Reed, DR / Price, RA et al. | 1993
- 1081
-
Dinucleotide repeat polymorphism at the human recoverin RCVI gene locus on chromosome 17pDollfus, H. / Rozet, J. -M. / Musarella, M. A. / Kaplan, J. / Munnich, A. et al. | 1993
- 1081-a
-
Dinucleotide repeat polymorphism at the D11S982E locusXiao, Hong / lde, Susan E. / Merril, Carl R. / Polymeropoulos, Mihael H. et al. | 1993
- 1082
-
Banl and Pvull polymorphisms in intron 2 of selection E (SELE)Powers, Patricia K. / Hixson, James E. et al. | 1993
- 1082-a
-
Dinucleotide repeat polymorphism at the locus D13S231Saksova, Ludmila / Hennies, Hans-Christian / Reis, André et al. | 1993
- 1082a
-
BanI and PvuII polymorphisms in intron 2 of selectin E (SELE)Powers, PK / Hixson, JE et al. | 1993
- 1083
-
A microsatellite polymorphism at the THRB locusBrett, Peter M. / Melmer, Georg / Robertson, Mary M. / Gurling, Hugh M.D. et al. | 1993
- 1083-a
-
A compound nucleotide repeat in the neurofibro-matosis (NF1) geneAndersen, Lone B. / Tarlé, Susan A. / Marchuk, Douglas A. / Legius, Eric / Collins, Francis S. et al. | 1993
- 1084
-
An EcoRI polymorphism in the AML1 geneBirn, Debbi J. / McKeithan, Timothy W. / Nucifora, Giuseppina et al. | 1993
- 1084-a
-
A dinucleotide repeat polymorphism in the human LAMB2 gene on chromosome 1qWatkins, H.C. / MacRae, C.A. / Thierfelder, L. / McKenna, W.J. / Seidman, C.E. / Seidman, J.G. et al. | 1993
- 1085
-
Dinucleotide repeat polymorphism at the D6S348 locusKansara, M.S. / Athwal, R.S. et al. | 1993
- 1085-a
-
Two consecutive dinucleotide repeats constitute an informative marker at the {alpha}1-antichymotrypsin (AACT) locusByth, Barbara C. / Cox, Diane W. et al. | 1993
- 1086
-
A Pstl polymorphism in the 3' end of the human type IV collagen alpha 3 chain (COL4A3) geneDelbridge, M.L. / Savige, J.A. et al. | 1993
- 1086a
-
A PstI polymorphism in the 3' end of the human type IV collagen alpha 3 chain (COL4A3) geneDelbridge, ML / Savige, JA et al. | 1993
- 1086-a
-
A CA dinucleotide polymorphism at D17S107 (17q12-q24)Barker, David F. / Nguyen, Kim / Fain, Pamela R. et al. | 1993
- 1087
-
Tetranucleotide repeat polymorphism at the D8S344 locusWard, Kenneth / Riley, Robyn / Lu, Jun / Robertson, Margaret / Nelson, Lesa et al. | 1993
- 1087-a
-
Length polymorphism within a complex dinucleotide repeat in the human decorin (DCN) geneD.Briggs, Michael / H.Cohn, Daniel et al. | 1993
- 1089
-
New human DNA polymorphisms submitted to the genome data base| 1993
- 1095
-
Author index| 1993