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1
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0017855558
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Partial 2p trisomy (p21 → pter) in two siblings of a family with a 2p-: 15q+ translocation
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Armendares, S., Salamanca-Gómez, F. (1978). Partial 2p trisomy (p21 → pter) in two siblings of a family with a 2p-: 15q+ translocation, Clin. Genet., 13, 17-24.
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Armendares, S.1
Salamanca-Gómez, F.2
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2
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0021025402
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Duplication of the distal segment of 14q
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Atkin, J.F., Patil, S. (1983). Duplication of the distal segment of 14q, Am. J. Med. Genet., 16, 357-366.
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Atkin, J.F.1
Patil, S.2
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3
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0021913560
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A child with a recombinant of chromosome 8 inherited from her carrier mother
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Barnes, I.C.S., Kumar, D., Bell, R.J.M. (1985). A child with a recombinant of chromosome 8 inherited from her carrier mother, J. Med. Genet., 22, 67-70.
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Barnes, I.C.S.1
Kumar, D.2
Bell, R.J.M.3
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4
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84907112223
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Ocular findings in partial trisomy 3q. A case report and review of the literature
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Chrousos, G.A., O'Neill, J.F., Traboulsi, E.I., Richmond, A., Rosenbaum, K.N. (1988). Ocular findings in partial trisomy 3q. A case report and review of the literature, Ophthal. Paediatr. Genet., 9, 127-130.
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Chrousos, G.A.1
O'Neill, J.F.2
Traboulsi, E.I.3
Richmond, A.4
Rosenbaum, K.N.5
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5
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0021667008
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Del(15)(q22q24) syndrome with Potter sequence
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Clark, R.D. (1984). Del(15)(q22q24) syndrome with Potter sequence, Am. J. Med. Genet., 19, 703-705.
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Clark, R.D.1
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6
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0016672834
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Trisomy 2q
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Dallapiccola, B., Forabosco, A., Calabro, A. (1975). Trisomy 2q, Acta. Genet. Med. Gemellol., 24, 307-310.
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Dallapiccola, B.1
Forabosco, A.2
Calabro, A.3
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7
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0018578308
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Complete and partial trisomy of different segments of chromosome 8: Case reports and review
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Fineman, R.M., Ablow, R.C., Breg, W.R., Wing, S.D., Rose, J.S., Rothman, S.L.G., Warpinski, J. (1979). Complete and partial trisomy of different segments of chromosome 8: case reports and review, Clin. Genet., 16, 390-398.
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Fineman, R.M.1
Ablow, R.C.2
Breg, W.R.3
Wing, S.D.4
Rose, J.S.5
Rothman, S.L.G.6
Warpinski, J.7
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8
-
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0024207171
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Interstitial deletion of chromosome 15: Two cases
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Formiga, L.D., Poenaru, L., Couronne, F., Flori, E., Eibel, J.L., Deminatti, M.M., Savary, J.B., Lai, J.L., Gilgenkrantz, S., Pierson, M. (1988). Interstitial deletion of chromosome 15: two cases, Hum. Genet., 80, 401-404.
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Formiga, L.D.1
Poenaru, L.2
Couronne, F.3
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Eibel, J.L.5
Deminatti, M.M.6
Savary, J.B.7
Lai, J.L.8
Gilgenkrantz, S.9
Pierson, M.10
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9
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0020043629
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Interstitial deletion of the long arm of chromosome 15
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Fryns, J.P., de Muelenaere, A., van den Berghe, H. (1982). Interstitial deletion of the long arm of chromosome 15, Ann. Genet. (Paris), 25, 59-60.
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Fryns, J.P.1
De Muelenaere, A.2
Van Den Berghe, H.3
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10
-
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0018236487
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Partial trisomy 8q resulting from maternal translocation t(2;8)(q373;q23)
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Giorgi, P.L., Tarantino, E., Formica, A., Cipriani, P., Dallapiccola, B. (1978). Partial trisomy 8q resulting from maternal translocation t(2;8)(q373;q23), Acta. Genet. Med. Gemollol., 27, 75-79.
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Giorgi, P.L.1
Tarantino, E.2
Formica, A.3
Cipriani, P.4
Dallapiccola, B.5
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11
-
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0029811521
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Structural chromosome anomalies in congenital diaphragmatic hernia
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Howe, D.T., Kilby, M.D., Sirry, H., Barker, G.M., Roberts, E., Davison, E.V., Mchugo, J., Whittle, M.J. (1996). Structural chromosome anomalies in congenital diaphragmatic hernia, Prenat. Diagn., 16, 1003-1009.
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Howe, D.T.1
Kilby, M.D.2
Sirry, H.3
Barker, G.M.4
Roberts, E.5
Davison, E.V.6
Mchugo, J.7
Whittle, M.J.8
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12
-
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0023618175
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Monosomy and trisomy of 15q24→qter in a family with a translocation t(6;15)(p25;q24)
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Kristoffersson, U., Heim, S., Mandahl, N., Sundkvist, L., Szelest, J., Hägerstrand, I. (1987). Monosomy and trisomy of 15q24→qter in a family with a translocation t(6;15)(p25;q24), Clin. Genet., 32, 169-171.
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Kristoffersson, U.1
Heim, S.2
Mandahl, N.3
Sundkvist, L.4
Szelest, J.5
Hägerstrand, I.6
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13
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0024418101
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Emerging phenotype of duplication (7p): A report of three cases and review of the literature
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Milunsky, J.M., Wyandt, H.E., Milunsky, A. (1989). Emerging phenotype of duplication (7p): a report of three cases and review of the literature, Am. J. Med. Genet., 33, 364-368.
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Milunsky, J.M.1
Wyandt, H.E.2
Milunsky, A.3
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14
-
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0017047723
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Chromosome 8 trisomy mosaic syndrome
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Mino, M., Kasubuchi, Y., Goto, M., Onouchi, Z., Kusunoki, T., Misawa, S., Abe, T. (1976). Chromosome 8 trisomy mosaic syndrome, Jap. J. Hum. Genet., 21, 69-78.
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Mino, M.1
Kasubuchi, Y.2
Goto, M.3
Onouchi, Z.4
Kusunoki, T.5
Misawa, S.6
Abe, T.7
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15
-
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0021795952
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Bilateral cystic nephroblastomas and multiple malformations with trisomy 8 mosaicism
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Nakamura, Y., Nakashima, H., Fukuda, S., Hashimoto, T., Maruyama, M. (1985). Bilateral cystic nephroblastomas and multiple malformations with trisomy 8 mosaicism, Hum. Pathol., 16, 754-756.
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Nakamura, Y.1
Nakashima, H.2
Fukuda, S.3
Hashimoto, T.4
Maruyama, M.5
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16
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0024419114
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Duplication of 16q and deletion of 15q
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Nyhan, W.L., Mascarello, J.M., Barshop, B., Doroski, D., Hirschhorn, K. (1989). Duplication of 16q and deletion of 15q, Am. J. Med. Genet., 34, 183-186.
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Nyhan, W.L.1
Mascarello, J.M.2
Barshop, B.3
Doroski, D.4
Hirschhorn, K.5
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17
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0015834643
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Tandem translocation 15/13
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Pasquali, F., Zuffardi, O., Severi, F., Colombo, A., Burgio, G.R. (1973). Tandem translocation 15/13, Ann. Genet. (Paris), 16, 47-50.
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Pasquali, F.1
Zuffardi, O.2
Severi, F.3
Colombo, A.4
Burgio, G.R.5
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