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1
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0016143839
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A case of ring chromosome E 17: 46,XX,r(17)(p13q25)
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in Japanese
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Ono K, Suzuki Y, Fujii I, Takeshita K, Arima M, Nakagome Y. A case of ring chromosome E 17: 46,XX,r(17)(p13q25). Jpn J Hum Genet 1974; 19: 235-42 (in Japanese)
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Ono, K.1
Suzuki, Y.2
Fujii, I.3
Takeshita, K.4
Arima, M.5
Nakagome, Y.6
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2
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0018636980
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Ring chromosome 17 in a mentally retarded boy
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Quazi QH, Madahar C, Kanchanapoomi R, Giridharan R, Beller E. Ring chromosome 17 in a mentally retarded boy. Ann Genet 1979; 22: 234-8
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Quazi, Q.H.1
Madahar, C.2
Kanchanapoomi, R.3
Giridharan, R.4
Beller, E.5
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3
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0019435755
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An infant with ring 17 chromosome and unusual dermatoglyphs: A new syndrome?
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Carpenter NJ, Leichtman LG, Stamper S, Say B. An infant with ring 17 chromosome and unusual dermatoglyphs: A new syndrome? Med Genet 1981; 18: 234-6
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Carpenter, N.J.1
Leichtman, L.G.2
Stamper, S.3
Say, B.4
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4
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0020034570
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Ring chromosome 17 in a mentally retarded young man - Clinical, cytogenic, and biochemical investigations
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Chudley AE, Pabello PD, McAlpine PJ, Nickel BE, Shokeir MHK. Ring chromosome 17 in a mentally retarded young man - Clinical, cytogenic, and biochemical investigations. Am J Med Genet 1982; 12: 219-25
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Chudley, A.E.1
Pabello, P.D.2
McAlpine, P.J.3
Nickel, B.E.4
Shokeir, M.H.K.5
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5
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0020540260
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The Miller-Dieker syndrome: Lissencephaly and monosomy 17p
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Dobyns WB, Stratton RF, Parke JT, Greenberg F, Nussbaum RL, Ledbetter DH. The Miller-Dieker syndrome: Lissencephaly and monosomy 17p. J Pediatr 1983; 102: 552-8
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Dobyns, W.B.1
Stratton, R.F.2
Parke, J.T.3
Greenberg, F.4
Nussbaum, R.L.5
Ledbetter, D.H.6
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7
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0025730003
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Miller-Dicker syndrome with ring chromosome 17
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Sharief N, Craze J, Summers D, Butler L, Wood CBS. Miller-Dicker syndrome with ring chromosome 17. Arch Dis Child 1991; 66: 710-2
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Sharief, N.1
Craze, J.2
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Butler, L.4
Wood, C.B.S.5
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9
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0027506860
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Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NFI)
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Wiktor A, Van Dyke DI., Weiss L. Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NFI). Am J Med Genet 1993; 45: 22-4
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Wiktor, A.1
Van Dyke, D.I.2
Weiss, L.3
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10
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0029151243
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Identification of a supernumerary marker derived from chromosome 17 using FISH
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Rosenberg C, Borovik CL, Canonaco RS, Sichero LC, Queiroz APS, Vianna-Morgante AM. Identification of a supernumerary marker derived from chromosome 17 using FISH. Am J Med Genet 1995; 59: 33-5
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Rosenberg, C.1
Borovik, C.L.2
Canonaco, R.S.3
Sichero, L.C.4
Queiroz, A.P.S.5
Vianna-Morgante, A.M.6
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11
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0031012229
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Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisation
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Morrison PJ, Smith NM, Martin KE, Young ID. Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisation. Am J Meal Genet 1997; 68: 50-3
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Morrison, P.J.1
Smith, N.M.2
Martin, K.E.3
Young, I.D.4
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12
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0019800346
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The cytogenetic and clinical implications of a ring chromosome 2
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Cote GB, Katsantonia A, Deligeorgis D. The cytogenetic and clinical implications of a ring chromosome 2. Ann Genet 1981; 24: 231-5
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Cote, G.B.1
Katsantonia, A.2
Deligeorgis, D.3
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