-
1
-
-
0033609907
-
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q
-
Cody JD, Ghidoni PD, DuPont BR, Hale DE, Hilsenbeck SG, Stratton RF, Hoffman DS, Muller S, Schaub RL, Leach RJ, Kaye CI (1999) Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q. Am J Med Genet 85:455-462
-
(1999)
Am J Med Genet
, vol.85
, pp. 455-462
-
-
Cody, J.D.1
Ghidoni, P.D.2
DuPont, B.R.3
Hale, D.E.4
Hilsenbeck, S.G.5
Stratton, R.F.6
Hoffman, D.S.7
Muller, S.8
Schaub, R.L.9
Leach, R.J.10
Kaye, C.I.11
-
2
-
-
0023711615
-
Classification of congenital aural atresia and results of reconstructive surgery
-
Cremers CWRJ, Teunissen E, Marres EHMA (1988) Classification of congenital aural atresia and results of reconstructive surgery. Adv Otorhinolaryngol 40:9-14
-
(1988)
Adv Otorhinolaryngol
, vol.40
, pp. 9-14
-
-
Cremers, C.W.R.J.1
Teunissen, E.2
Marres, E.H.M.A.3
-
4
-
-
18344392245
-
Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas
-
Hodgson G, Hager JH, Volik S, Hariono S, Wernick M, Moore D, Nowak N, Albertson DG, Pinkel D, Collins C, Hanahan D, Gray JW (2001) Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas. Nat Genet 29:459-464
-
(2001)
Nat Genet
, vol.29
, pp. 459-464
-
-
Hodgson, G.1
Hager, J.H.2
Volik, S.3
Hariono, S.4
Wernick, M.5
Moore, D.6
Nowak, N.7
Albertson, D.G.8
Pinkel, D.9
Collins, C.10
Hanahan, D.11
Gray, J.W.12
-
5
-
-
0344564142
-
Cloning and characterization of ZNF236, a glucose-regulated Kruppel-like zinc-finger gene mapping to human chromosome 18q22-q23
-
Holmes DI, Wahab NA, Mason RM (1999) Cloning and characterization of ZNF236, a glucose-regulated Kruppel-like zinc-finger gene mapping to human chromosome 18q22-q23. Genomics 60:105-109
-
(1999)
Genomics
, vol.60
, pp. 105-109
-
-
Holmes, D.I.1
Wahab, N.A.2
Mason, R.M.3
-
6
-
-
0037097358
-
Association of external auditory canal atresia, vertical talus, and hypertelorism: Confirmation of Rasmussen syndrome
-
Julia S, Pedespan JM, Boudard Ph, Barbier R, Gavilan-Cellie I, Chateil JF, Lacombe D (2002) Association of external auditory canal atresia, vertical talus, and hypertelorism: confirmation of Rasmussen syndrome. Am J Med Genet 110:179-181
-
(2002)
Am J Med Genet
, vol.110
, pp. 179-181
-
-
Julia, S.1
Pedespan, J.M.2
Boudard, P.H.3
Barbier, R.4
Gavilan-Cellie, I.5
Chateil, J.F.6
Lacombe, D.7
-
7
-
-
0032513589
-
Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss
-
Keppler-Noreuil KM, Carroll AJ, Finley SC, Descartes M, Cody JD, DuPont BR, Gay CT Leach RJ (1998) Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss. Am J Med Genet 76:372-378
-
(1998)
Am J Med Genet
, vol.76
, pp. 372-378
-
-
Keppler-Noreuil, K.M.1
Carroll, A.J.2
Finley, S.C.3
Descartes, M.4
Cody, J.D.5
DuPont, B.R.6
Gay, C.T.7
Leach, R.J.8
-
8
-
-
0027422825
-
Molecular analysis of the 18q- syndrome - And correlation with phenotype
-
Kline AD, White ME, Wapner R, Rojas K, Biesecker LG, Kamholz J, Zackai EH, Muenke M, Scott CI Jr, Overhauser J (1993) Molecular analysis of the 18q- syndrome - and correlation with phenotype. Am J Hum Genet 52:895-906
-
(1993)
Am J Hum Genet
, vol.52
, pp. 895-906
-
-
Kline, A.D.1
White, M.E.2
Wapner, R.3
Rojas, K.4
Biesecker, L.G.5
Kamholz, J.6
Zackai, E.H.7
Muenke, M.8
Scott C.I., Jr.9
Overhauser, J.10
-
9
-
-
0033372913
-
SALL3, a new member of the human spalt-like gene family, maps to 18q23
-
Kohlhase J, Hausmann S, Stojmenovic G, Dixkens C, Bink K, Schulz-Schaeffer W, Altmann M, Engel W (1999) SALL3, a new member of the human spalt-like gene family, maps to 18q23. Genomics 62:216-222
-
(1999)
Genomics
, vol.62
, pp. 216-222
-
-
Kohlhase, J.1
Hausmann, S.2
Stojmenovic, G.3
Dixkens, C.4
Bink, K.5
Schulz-Schaeffer, W.6
Altmann, M.7
Engel, W.8
-
10
-
-
0032431034
-
Structural organization and chromosomal localization of three human galanin receptor genes
-
Lismaa TP, Fathi Z, Hort YJ, Iben LG, Dutton JL, Baker E, Sutherland GR, Shine J (1998) Structural organization and chromosomal localization of three human galanin receptor genes. Ann NY Acad Sci 863:56-63
-
(1998)
Ann NY Acad Sci
, vol.863
, pp. 56-63
-
-
Lismaa, T.P.1
Fathi, Z.2
Hort, Y.J.3
Iben, L.G.4
Dutton, J.L.5
Baker, E.6
Sutherland, G.R.7
Shine, J.8
-
11
-
-
0018589660
-
External ear malformations: Epidemiology, genetics, and natural history
-
Melnick M, Myranthopoulos NC, Paul NW (1979) External ear malformations: epidemiology, genetics, and natural history. Birth Defects Orig Artic Ser 15:1-140
-
(1979)
Birth Defects Orig Artic Ser
, vol.15
, pp. 1-140
-
-
Melnick, M.1
Myranthopoulos, N.C.2
Paul, N.W.3
-
12
-
-
85031167788
-
Congenital aural atresia in 18q deletion or de Grouchy syndrome
-
in press
-
Nuijten I, Admiraal R, van Buggenhout G, Cremers C, Frijns JP, Smeets D, van Ravenswaaij-Arts C. Congenital aural atresia in 18q deletion or de Grouchy syndrome. Otol Neurotol (in press)
-
Otol Neurotol
-
-
Nuijten, I.1
Admiraal, R.2
Van Buggenhout, G.3
Cremers, C.4
Frijns, J.P.5
Smeets, D.6
Van Ravenswaaij-Arts, C.7
-
13
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
Pinkel D, Segraves R, Sudar D, Clark S, Poole I, Kowbel D, Collins C, Kuo WL, Chen C, Zhai Y, Dairkee SH, Ljung BM, Gray JW, Albertson DG (1998) High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet 20:207-211
-
(1998)
Nat Genet
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
Clark, S.4
Poole, I.5
Kowbel, D.6
Collins, C.7
Kuo, W.L.8
Chen, C.9
Zhai, Y.10
Dairkee, S.H.11
Ljung, B.M.12
Gray, J.W.13
Albertson, D.G.14
-
14
-
-
0036898231
-
Characterizing the physical genome
-
Pollack JR, Iyer VR (2002) Characterizing the physical genome. Nat Genet 32:S515-S521
-
(2002)
Nat Genet
, vol.32
-
-
Pollack, J.R.1
Iyer, V.R.2
-
16
-
-
0025827836
-
Interstitial deletion of the long arm of chromosome 18, del(18) (q12.2q21.1): A report of three cases of an autosomal deletion with a mild phenotype
-
Schinzel A, Binkert F, Lillington DM, Sands M, Stocks RJ, Lindenbaum RH, Matthews H, Sheridan H (1991) Interstitial deletion of the long arm of chromosome 18, del(18) (q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype. J Med Genet 28:352-355
-
(1991)
J Med Genet
, vol.28
, pp. 352-355
-
-
Schinzel, A.1
Binkert, F.2
Lillington, D.M.3
Sands, M.4
Stocks, R.J.5
Lindenbaum, R.H.6
Matthews, H.7
Sheridan, H.8
-
17
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
Solinas-Toldo S, Lampel S, Stilgenbauer S, Nickolenko J, Benner A, Dohner H, Cremer T, Lichter P (1997) Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chrom Cancer 20:399-407
-
(1997)
Genes Chrom Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
Lampel, S.2
Stilgenbauer, S.3
Nickolenko, J.4
Benner, A.5
Dohner, H.6
Cremer, T.7
Lichter, P.8
-
18
-
-
0030900735
-
Molecular characterization of patients with 18q23 deletions
-
Strathdee G, Sutherland R, Jonsson JJ, Sataloff R, Kohonen-Corish M, Grady D, Overhauser J (1997) Molecular characterization of patients with 18q23 deletions. Am J Hum Genet 60:860-868
-
(1997)
Am J Hum Genet
, vol.60
, pp. 860-868
-
-
Strathdee, G.1
Sutherland, R.2
Jonsson, J.J.3
Sataloff, R.4
Kohonen-Corish, M.5
Grady, D.6
Overhauser, J.7
-
19
-
-
0028871377
-
Analysis of clinical variation seen in patients with 18q terminal deletions
-
Strathdee G, Zackai EH, Shapiro R, Kamholz J, Overhauser J (1995) Analysis of clinical variation seen in patients with 18q terminal deletions. Am J Med Genet 59:476-483
-
(1995)
Am J Med Genet
, vol.59
, pp. 476-483
-
-
Strathdee, G.1
Zackai, E.H.2
Shapiro, R.3
Kamholz, J.4
Overhauser, J.5
-
20
-
-
0026736251
-
Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
-
Telenius H, Carter NP, Bebb CE, Nordenskjold M, Ponder BA, Tunnacliffe A (1992) Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 13:718-725
-
(1992)
Genomics
, vol.13
, pp. 718-725
-
-
Telenius, H.1
Carter, N.P.2
Bebb, C.E.3
Nordenskjold, M.4
Ponder, B.A.5
Tunnacliffe, A.6
-
21
-
-
18344379676
-
High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization
-
Veltman JA, Schoenmakers EFPM, Eussen BH, Janssen I, Merkx G, van Cleef B, van Ravenswaaij CM, Brunner HG, Smeets D, Geurts van Kessel A (2002) High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization. Am J Hum Genet 70:1269-1276
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1269-1276
-
-
Veltman, J.A.1
Schoenmakers, E.F.P.M.2
Eussen, B.H.3
Janssen, I.4
Merkx, G.5
Van Cleef, B.6
Van Ravenswaaij, C.M.7
Brunner, H.G.8
Smeets, D.9
Geurts Van Kessel, A.10
-
22
-
-
0026076170
-
Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion
-
Weiss BJ, Kamholz J, Ritter A, Zackai EH, McDonald-McGinn DM, Emanuel B, Fischbeck KH (1991) Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion. Ann Neurol 30:419-423
-
(1991)
Ann Neurol
, vol.30
, pp. 419-423
-
-
Weiss, B.J.1
Kamholz, J.2
Ritter, A.3
Zackai, E.H.4
McDonald-McGinn, D.M.5
Emanuel, B.6
Fischbeck, K.H.7
-
23
-
-
0036173663
-
Array based CGH for the differential diagnosis of renal cell cancer
-
Wilhelm M, Veltman JA, Olshen A, Jain A, Moore DH, Kovacs G, Presti JC, Waldman FM (2002) Array based CGH for the differential diagnosis of renal cell cancer. Cancer Res 62:957-960
-
(2002)
Cancer Res
, vol.62
, pp. 957-960
-
-
Wilhelm, M.1
Veltman, J.A.2
Olshen, A.3
Jain, A.4
Moore, D.H.5
Kovacs, G.6
Presti, J.C.7
Waldman, F.M.8
-
24
-
-
0018630218
-
Syndromes associated with deletion of the long arm of chromosome 18 [del(18q)]
-
Wilson MG, Towner JW, Forsman I, Siris E (1979) Syndromes associated with deletion of the long arm of chromosome 18 [del(18q)]. Am J Med Genet 3:155-174
-
(1979)
Am J Med Genet
, vol.3
, pp. 155-174
-
-
Wilson, M.G.1
Towner, J.W.2
Forsman, I.3
Siris, E.4
|