-
1
-
-
0014706722
-
The syndrome of the metacentric microchromosome
-
Abbo G, Zellweger H. 1970. The syndrome of the metacentric microchromosome. Helv Paediatr Acta 25:83-94.
-
(1970)
Helv Paediatr Acta
, vol.25
, pp. 83-94
-
-
Abbo, G.1
Zellweger, H.2
-
2
-
-
0027212895
-
Isochromosome 18p in a mother and her child
-
Abeliovich D, Dagan J, Levy A, Steinberg A, Zlotogora J. 1993. Isochromosome 18p in a mother and her child. Am J Med Genet 46:392-393.
-
(1993)
Am J Med Genet
, vol.46
, pp. 392-393
-
-
Abeliovich, D.1
Dagan, J.2
Levy, A.3
Steinberg, A.4
Zlotogora, J.5
-
3
-
-
0028337766
-
De novo isochromosome 18p in two patients: Cytogenetic diagnosis and confirmation by chromosome painting
-
Back E, Toder R, Voiculescu I, Wildberg A, Schempp W. 1994. De novo isochromosome 18p in two patients: Cytogenetic diagnosis and confirmation by chromosome painting. Clin Genet 45:301-304.
-
(1994)
Clin Genet
, vol.45
, pp. 301-304
-
-
Back, E.1
Toder, R.2
Voiculescu, I.3
Wildberg, A.4
Schempp, W.5
-
5
-
-
0035370539
-
Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters
-
Boyle J, Sangha K, Dill F, Robinson WP, Yong SL. 2001. Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters. Am J Med Genet 101:65-69.
-
(2001)
Am J Med Genet
, vol.101
, pp. 65-69
-
-
Boyle, J.1
Sangha, K.2
Dill, F.3
Robinson, W.P.4
Yong, S.L.5
-
6
-
-
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, Tommerup N, Brondum-Nielson K. 1996. Tetrasomy 18p de novo: Parental origin and different mechanisms of formation. Eur J Hum Genet 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
Tommerup, N.15
Brondum-Nielson, K.16
-
7
-
-
0025007098
-
The isochromosome 18p syndrome: Confirmation of cytogenetic diagnosis in nine cases by in situ hybridization
-
Callen DF, Freemantle CJ, Ringenbergs ML, Baker E, Eyre HJ, Romain D, Haan EA. 1990. The isochromosome 18p syndrome: Confirmation of cytogenetic diagnosis in nine cases by in situ hybridization. Am J Hum Genet 47:493-498.
-
(1990)
Am J Hum Genet
, vol.47
, pp. 493-498
-
-
Callen, D.F.1
Freemantle, C.J.2
Ringenbergs, M.L.3
Baker, E.4
Eyre, H.J.5
Romain, D.6
Haan, E.A.7
-
8
-
-
0018569779
-
A gene for hypospadias in a child with presumed tetrasomy 18p
-
Cote GB, Petmezaki S, Bastakis N. 1979. A gene for hypospadias in a child with presumed tetrasomy 18p. Am J Med Genet 4:141-146.
-
(1979)
Am J Med Genet
, vol.4
, pp. 141-146
-
-
Cote, G.B.1
Petmezaki, S.2
Bastakis, N.3
-
9
-
-
0030844677
-
Tetrasomy 18p caused by paternal meiotic nondisjunction
-
Eggermann T, Engels H, Apacik C, Moskalonek B, Muller-Navia J, Schwanitz G. Stengel-Rutkowski S. 1997. Tetrasomy 18p caused by paternal meiotic nondisjunction. Eur J Hum Genet 5:175-177.
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 175-177
-
-
Eggermann, T.1
Engels, H.2
Apacik, C.3
Moskalonek, B.4
Muller-Navia, J.5
Schwanitz, G.6
Stengel-Rutkowski, S.7
-
10
-
-
0028588455
-
Tetrasomy 18p in two cases confirmation by in situ hybridization
-
Esmer MC, Prias S, Gomez L, Carnevale A. 1994. Tetrasomy 18p in two cases confirmation by in situ hybridization. Ann Genet 37:156-159.
-
(1994)
Ann Genet
, vol.37
, pp. 156-159
-
-
Esmer, M.C.1
Prias, S.2
Gomez, L.3
Carnevale, A.4
-
11
-
-
0026882258
-
A comparison of two approaches for identifying reinforcers for persons with severe and profound disabilities
-
Fisher W, Piazza CC, Bowman LG, Hagopian LP, Owens JC, Slevin I. 1992. A comparison of two approaches for identifying reinforcers for persons with severe and profound disabilities. J Appl Behav Anal 25:491-498.
-
(1992)
J Appl Behav Anal
, vol.25
, pp. 491-498
-
-
Fisher, W.1
Piazza, C.C.2
Bowman, L.G.3
Hagopian, L.P.4
Owens, J.C.5
Slevin, I.6
-
12
-
-
0032163991
-
Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism
-
Habecker-Green JG, Naeem R, Gold H, O'Grady JP, Kanaan C, Bayer-Zwirello L, Murray MS, Cohn GM. 1998. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism. J Perinatol 18:395-398.
-
(1998)
J Perinatol
, vol.18
, pp. 395-398
-
-
Habecker-Green, J.G.1
Naeem, R.2
Gold, H.3
O'Grady, J.P.4
Kanaan, C.5
Bayer-Zwirello, L.6
Murray, M.S.7
Cohn, G.M.8
-
13
-
-
0023005791
-
Trisomy (18q) and tetrasomy (18p) resulting from isochromosome formation
-
Kleczkowska A, Fryns JP, Buttiens M, de Bisschop F, Emmery L, Van den Berghe H. 1986. Trisomy (18q) and tetrasomy (18p) resulting from isochromosome formation. Clin Genet 30:503-508.
-
(1986)
Clin Genet
, vol.30
, pp. 503-508
-
-
Kleczkowska, A.1
Fryns, J.P.2
Buttiens, M.3
De Bisschop, F.4
Emmery, L.5
Van Den Berghe, H.6
-
14
-
-
0027272904
-
Confirmation of isochromosome 18p using whole chromosome arm-specific fluorescence in situ hybridization
-
Mewar R, Harrison W, Overhauser J. 1993. Confirmation of isochromosome 18p using whole chromosome arm-specific fluorescence in situ hybridization. Cytogenet Cell Genet 64:1-4.
-
(1993)
Cytogenet Cell Genet
, vol.64
, pp. 1-4
-
-
Mewar, R.1
Harrison, W.2
Overhauser, J.3
-
15
-
-
0026001668
-
Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomes
-
Park VM, Gustashaw KM, Bilenker RM, Golden WL. 1991. Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomes. Am J Med Genet 41:180-183.
-
(1991)
Am J Med Genet
, vol.41
, pp. 180-183
-
-
Park, V.M.1
Gustashaw, K.M.2
Bilenker, R.M.3
Golden, W.L.4
-
16
-
-
0021205828
-
Tetrasomy 18p: A distinctive syndrome
-
Rivera H, Moller M, Hernandez A, Enriquez-Guerra MA, Arreola R, Cantu JM. 1984. Tetrasomy 18p: A distinctive syndrome. Ann Genet 27:187-189.
-
(1984)
Ann Genet
, vol.27
, pp. 187-189
-
-
Rivera, H.1
Moller, M.2
Hernandez, A.3
Enriquez-Guerra, M.A.4
Arreola, R.5
Cantu, J.M.6
-
17
-
-
0025350269
-
Tetrasomy 18p in a child with trisomy 18 phenotype
-
Singer TS, Kohn G, Yatziv S. 1990. Tetrasomy 18p in a child with trisomy 18 phenotype. Am J Med Genet 36:144-147.
-
(1990)
Am J Med Genet
, vol.36
, pp. 144-147
-
-
Singer, T.S.1
Kohn, G.2
Yatziv, S.3
-
18
-
-
0024520943
-
Sibs with tetrasomy 18p born to a mother with trisomy 18p
-
Takeda K, Okamura T, Hasegawa T. 1989. Sibs with tetrasomy 18p born to a mother with trisomy 18p. J Med Genet 26:195-197.
-
(1989)
J Med Genet
, vol.26
, pp. 195-197
-
-
Takeda, K.1
Okamura, T.2
Hasegawa, T.3
-
19
-
-
0016664827
-
Origin of a small metacentric chromosome: Familial and cytogenic evidence
-
Taylor KM, Wolfinger HL, Brown MG, Chadwick DL. 1975. Origin of a small metacentric chromosome: Familial and cytogenic evidence. Clin Genet 8:364-369.
-
(1975)
Clin Genet
, vol.8
, pp. 364-369
-
-
Taylor, K.M.1
Wolfinger, H.L.2
Brown, M.G.3
Chadwick, D.L.4
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