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1
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0023816091
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A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4
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Beall MH, Falk RE, Ying KL. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4 Am J Med Genet 1988: 31: 553-557.
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Beall, M.H.1
Falk, R.E.2
Ying, K.L.3
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2
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0023127497
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A new interstitial deletion of chromosome no. 4: Del(4)(q22::q25)
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Butler LJ, Palmer AV, Spencer T, Tabios-Broadway R, Wall WJ. A new interstitial deletion of chromosome no. 4: del(4)(q22::q25). Clin Genet 1987: 31: 199-205.
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Butler, L.J.1
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Tabios-Broadway, R.4
Wall, W.J.5
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3
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0028135127
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A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia
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Calabrese G, Guanciali Franchi P, Stuppia L, Mingarelli R, Rossi C, Ramenghi L, Marino M, Morizio E, Peila R, Antonucci A, Palka G. A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. J Med Genet 1994: 31: 804-806.
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Calabrese, G.1
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Stuppia, L.3
Mingarelli, R.4
Rossi, C.5
Ramenghi, L.6
Marino, M.7
Morizio, E.8
Peila, R.9
Antonucci, A.10
Palka, G.11
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4
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0022452379
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Interstitial deletion of chromosome 4q diagnosed prenatally
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Campbell JM, Williams J, Batcup G. Interstitial deletion of chromosome 4q diagnosed prenatally. J Med Genet 1986: 23: 366-369.
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Campbell, J.M.1
Williams, J.2
Batcup, G.3
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5
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0028947787
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Brief clinical report: Interstitial deletion of the long arm of chromosome 4, del(4)(q28→q31.3)
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Copelli S, del Rey G, Heinrich J, Coco R. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28→q31.3). Am J Med Genet 1995: 55: 77-79.
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Copelli, S.1
Del Rey, G.2
Heinrich, J.3
Coco, R.4
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6
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0025105098
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Interstitial deletion of chromosome 4 del(4)(q12q21.1), in a child with multiple congenital abnormalities
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Curtis M, Quarrell O, Cobon A, Cummins M. Interstitial deletion of chromosome 4 del(4)(q12q21.1), in a child with multiple congenital abnormalities. J Med Genet 1990: 27: 64-65.
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Curtis, M.1
Quarrell, O.2
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Cummins, M.4
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7
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0024370425
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Terminal deletion 4q in a severely retarded boy
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de Michelena MI, Campos PJ. Terminal deletion 4q in a severely retarded boy. Am J Med Genet 1989: 33: 228-230.
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De Michelena, M.I.1
Campos, P.J.2
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8
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0028859381
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Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4
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Fang YY, Eyre HJ, Bohlander SK, Estop A, McPherson E, Trager T, Riess O, Callen DF. Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4. Am J Hum Genet 1989: 57: 1137-1142.
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Fang, Y.Y.1
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Bohlander, S.K.3
Estop, A.4
McPherson, E.5
Trager, T.6
Riess, O.7
Callen, D.F.8
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9
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0025959476
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Ring chromosome 4 in a child with mild dysmorphic signs
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Freyberger G, Wamsler C, Schmid M. Ring chromosome 4 in a child with mild dysmorphic signs. Clin Genet 1991: 39: 151-155.
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Freyberger, G.1
Wamsler, C.2
Schmid, M.3
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11
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0025074747
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Ring chromosome 4 in a child with duodenal atresia
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Halal F, Vekemans M. Ring chromosome 4 in a child with duodenal atresia. Am J Med Genet 1990: 37: 79-82.
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Halal, F.1
Vekemans, M.2
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12
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0022901522
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A terminal deletion of the long arm of chromosome 4, 46,XX,del(4)(q33), in an infant with phenotypic features of Williams syndrome
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Jefferson RD, Burn J, Gaunt KL, Hunter S, Davison EV. A terminal deletion of the long arm of chromosome 4, 46,XX,del(4)(q33), in an infant with phenotypic features of Williams syndrome. J Med Genet 1986: 23: 474-480.
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Jefferson, R.D.1
Burn, J.2
Gaunt, K.L.3
Hunter, S.4
Davison, E.V.5
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13
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0023792118
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Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes
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Lin AE, Gaver KL, Diggans G, Clemens M, Wenger SL, Steele MW, Jones MC, Israel J. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes. Am J Med Genet 1988: 31: 533-548.
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Lin, A.E.1
Gaver, K.L.2
Diggans, G.3
Clemens, M.4
Wenger, S.L.5
Steele, M.W.6
Jones, M.C.7
Israel, J.8
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14
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0026771543
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The presence of interstitial telomeric sequences in constitutional chromosome abnormalities
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Park VM, Gustashaw KM, Wathen TM. The presence of interstitial telomeric sequences in constitutional chromosome abnormalities. Am J Hum Genet 1992: 50: 914-923.
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Park, V.M.1
Gustashaw, K.M.2
Wathen, T.M.3
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15
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0027303944
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Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability
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Pezzolo A, Gimelli G, Cohen A, Lavaggetto A, Romano C, Fogu G, Zuffardi O. Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability. Hum Genet 1993: 92: 23-27.
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Pezzolo, A.1
Gimelli, G.2
Cohen, A.3
Lavaggetto, A.4
Romano, C.5
Fogu, G.6
Zuffardi, O.7
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16
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0025756294
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Second case report of del(4)(q25q27) and review of the literature
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Raczenbek C, Krassikoff N, Cosper P. Second case report of del(4)(q25q27) and review of the literature. Clin Genet 1991: 39: 463-466.
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Raczenbek, C.1
Krassikoff, N.2
Cosper, P.3
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17
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0026528252
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Interstitial deletion of the distal long arm of chromosome 4
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Sarda P, Lefort G, Fryns JP, Humeau C, Rieu D. Interstitial deletion of the distal long arm of chromosome 4. J Med Genet 1992: 29: 259-261.
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Sarda, P.1
Lefort, G.2
Fryns, J.P.3
Humeau, C.4
Rieu, D.5
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18
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0020444095
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Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33
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Tomkins DJ, Hunter AGW, Uchida IA, Roberts MH. Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33. Clin Genet 1982: 22: 348-355.
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Tomkins, D.J.1
Hunter, A.G.W.2
Uchida, I.A.3
Roberts, M.H.4
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19
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0027080773
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Constitutional ring chromosomes and tumour suppressor genes
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Tommerup N, Lothe R. Constitutional ring chromosomes and tumour suppressor genes. J Med Genet 1992: 29: 879-882.
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Tommerup, N.1
Lothe, R.2
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