-
1
-
-
0030036635
-
Tetrasomy 18p de novo: Parental origin and different mechanisms of formation
-
Bugge M, Blennow E, Friedrich U, Petersen MB, Pedeutour F, Tsezou A, Orum A, Hermann S, Lyngbye T, Sarri C, Avramopoulos D, Kitsiou S, Lambert JC, Guzda M, Tomerup N, Brondum-Nielsen K: Tetrasomy 18p de novo: Parental origin and different mechanisms of formation. Eur J Hum Genet 1996;4:160-167.
-
(1996)
Eur J Hum Genet
, vol.4
, pp. 160-167
-
-
Bugge, M.1
Blennow, E.2
Friedrich, U.3
Petersen, M.B.4
Pedeutour, F.5
Tsezou, A.6
Orum, A.7
Hermann, S.8
Lyngbye, T.9
Sarri, C.10
Avramopoulos, D.11
Kitsiou, S.12
Lambert, J.C.13
Guzda, M.14
Tomerup, N.15
Brondum-Nielsen, K.16
-
2
-
-
0030012071
-
Tetrasomy 18p de novo: Identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing
-
Eggermann T, Engels H, Moskalonek B, Nöthen MM, Müller-Navia J, Schleiermacher E, Schwanitz G, Stengel-Rutkowski S: Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing. Hum Genet 1996;97: 568-572.
-
(1996)
Hum Genet
, vol.97
, pp. 568-572
-
-
Eggermann, T.1
Engels, H.2
Moskalonek, B.3
Nöthen, M.M.4
Müller-Navia, J.5
Schleiermacher, E.6
Schwanitz, G.7
Stengel-Rutkowski, S.8
-
3
-
-
0030015733
-
Isochromosomes 18p result from maternal meiosis II nondisjunction
-
Kotzot D, Bundscherer G, Bernasconi F, Brecevic L, Lurie I, Basaran S, Baccicchetti C, Höller A, Castellan C, Braun-Quentin C, Pfeiffer RA, Schinzel A: Isochromosomes 18p result from maternal meiosis II nondisjunction. Eur J Hum Genet 1996;4:168-174.
-
(1996)
Eur J Hum Genet
, vol.4
, pp. 168-174
-
-
Kotzot, D.1
Bundscherer, G.2
Bernasconi, F.3
Brecevic, L.4
Lurie, I.5
Basaran, S.6
Baccicchetti, C.7
Höller, A.8
Castellan, C.9
Braun-Quentin, C.10
Pfeiffer, R.A.11
Schinzel, A.12
-
4
-
-
0030064773
-
Trisomy of human chromosome 18: Molecular studies on parental origin and cell stage of nondisjunction
-
Eggermann T, Nöthen MM, Eiben B, Hofmann D, Hinkel K, Fimmers R, Schwanitz G: Trisomy of human chromosome 18: Molecular studies on parental origin and cell stage of nondisjunction. Hum Genet 1996;97:218-223.
-
(1996)
Hum Genet
, vol.97
, pp. 218-223
-
-
Eggermann, T.1
Nöthen, M.M.2
Eiben, B.3
Hofmann, D.4
Hinkel, K.5
Fimmers, R.6
Schwanitz, G.7
-
5
-
-
0028907505
-
Trisomy 18: Studies on parents and cell division of origin and the effect of aberrant recombination on nondisjunction
-
Fisher JM, Harvey JF, Morton NE, Jacobs PA: Trisomy 18: Studies on parents and cell division of origin and the effect of aberrant recombination on nondisjunction. Am J Hum Genet 1995;56:669-675.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 669-675
-
-
Fisher, J.M.1
Harvey, J.F.2
Morton, N.E.3
Jacobs, P.A.4
-
6
-
-
0022627760
-
The heteromorphic on chromosome 18 using restriction endonuclease Alul
-
Babu A, Verma RS: The heteromorphic on chromosome 18 using restriction endonuclease Alul. Am J Hum Genet 1986;38:549-554.
-
(1986)
Am J Hum Genet
, vol.38
, pp. 549-554
-
-
Babu, A.1
Verma, R.S.2
-
8
-
-
0023740562
-
Origin of the extra chromosome in trisomy 18
-
Kondoh T, Tonoki H, Matsumoto T, Tsukahara M, Niikawa N: Origin of the extra chromosome in trisomy 18. Hum Genet 1988;79:377-378.
-
(1988)
Hum Genet
, vol.79
, pp. 377-378
-
-
Kondoh, T.1
Tonoki, H.2
Matsumoto, T.3
Tsukahara, M.4
Niikawa, N.5
-
9
-
-
0024432089
-
Parental origin of the extra chromosome in trisomy 18
-
Kupke KG, Müller U: Parental origin of the extra chromosome in trisomy 18. Am J Hum Genet 1989;45:599-605.
-
(1989)
Am J Hum Genet
, vol.45
, pp. 599-605
-
-
Kupke, K.G.1
Müller, U.2
-
10
-
-
0027216939
-
Parental origin of the supernumerary chromosome in trisomy 18
-
Ya-gang X, Robinson WP, Spiegel R, Binkert F, Ruefenacht U, Schinzel AA: Parental origin of the supernumerary chromosome in trisomy 18. Clin Genet 1993;44:57-71.
-
(1993)
Clin Genet
, vol.44
, pp. 57-71
-
-
Ya-gang, X.1
Robinson, W.P.2
Spiegel, R.3
Binkert, F.4
Ruefenacht, U.5
Schinzel, A.A.6
-
11
-
-
0028233254
-
Delineation of marker chromosomes by reverse chromosome painting using only two DOP-PCR amplified microdissected chromosomes
-
Viersbach R, Schwanitz G, Nöthen MM: Delineation of marker chromosomes by reverse chromosome painting using only two DOP-PCR amplified microdissected chromosomes. Hum Genet 1994;93:663-667.
-
(1994)
Hum Genet
, vol.93
, pp. 663-667
-
-
Viersbach, R.1
Schwanitz, G.2
Nöthen, M.M.3
-
12
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF: A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;16:1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
13
-
-
0027161022
-
Mutation of human short tandem repeats
-
Weber JL, Wong C: Mutation of human short tandem repeats. Hum Mol Genet 1993;2: 1123-1128.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1123-1128
-
-
Weber, J.L.1
Wong, C.2
-
14
-
-
0028921591
-
Integration of the 1993-94 Généthon genetic linkage map for chromosome 18 with the physical map using a somatic cell hybrid mapping panel
-
Rojas K, Silverman GA, Hudson JR, Overhauser J: Integration of the 1993-94 Généthon genetic linkage map for chromosome 18 with the physical map using a somatic cell hybrid mapping panel. Genomics 1995;25:329-330.
-
(1995)
Genomics
, vol.25
, pp. 329-330
-
-
Rojas, K.1
Silverman, G.A.2
Hudson, J.R.3
Overhauser, J.4
-
15
-
-
0027447719
-
Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age
-
Antonarakis SE, Avramopoulos D, Blouin JL, Talbot CC Jr, Schinzel AA: Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age. Nature Genet 1993;3:146-150.
-
(1993)
Nature Genet
, vol.3
, pp. 146-150
-
-
Antonarakis, S.E.1
Avramopoulos, D.2
Blouin, J.L.3
Talbot Jr., C.C.4
Schinzel, A.A.5
-
17
-
-
0027937004
-
Nondisjunction of human acrocentric chromosomes studies of 432 trisomie fetuses and liveborns
-
Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherma S, Hassold T: Nondisjunction of human acrocentric chromosomes studies of 432 trisomie fetuses and liveborns. Hum Genet 1994;94:411-417.
-
(1994)
Hum Genet
, vol.94
, pp. 411-417
-
-
Zaragoza, M.V.1
Jacobs, P.A.2
James, R.S.3
Rogan, P.4
Sherma, S.5
Hassold, T.6
-
18
-
-
0027139205
-
Report of the Second International Workshop on Human Chromosome 18 Mapping
-
vanKessel AG, Straub RE, Silverman GA, Gerken S, Overhauser J: Report of the Second International Workshop on Human Chromosome 18 Mapping. Cytogenet Cell Genet 1994; 65:142-163.
-
(1994)
Cytogenet Cell Genet
, vol.65
, pp. 142-163
-
-
VanKessel, A.G.1
Straub, R.E.2
Silverman, G.A.3
Gerken, S.4
Overhauser, J.5
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