-
1
-
-
0015865998
-
A new case of trisomy for the short arm no 9 chromosome
-
Baccichetti C, Tenconi R. 1973. A new case of trisomy for the short arm no 9 chromosome. J Med Genet 10:296-299.
-
(1973)
J Med Genet
, vol.10
, pp. 296-299
-
-
Baccichetti, C.1
Tenconi, R.2
-
2
-
-
0018597220
-
Partial trisomy 9: Clinical and cytogenetic correlations
-
Baccichetti C, Lenzini E, Temperani P, Pallotta R, Giorgi PL, Tarantino E, Mengarda G, Dordi B. 1979. Partial trisomy 9: clinical and cytogenetic correlations. Ann Genet 22:199-204.
-
(1979)
Ann Genet
, vol.22
, pp. 199-204
-
-
Baccichetti, C.1
Lenzini, E.2
Temperani, P.3
Pallotta, R.4
Giorgi, P.L.5
Tarantino, E.6
Mengarda, G.7
Dordi, B.8
-
3
-
-
0017104032
-
Possible intrachromosomal duplication in a case of trisomy 9p
-
Chiyo H, Furuyama J, Suehara N, Obashi Y, Kikkawa H and Ikoma F. 1976. Possible intrachromosomal duplication in a case of trisomy 9p. Hum Genet 34:217-221.
-
(1976)
Hum Genet
, vol.34
, pp. 217-221
-
-
Chiyo, H.1
Furuyama, J.2
Suehara, N.3
Obashi, Y.4
Kikkawa, H.5
Ikoma, F.6
-
4
-
-
0019969739
-
Duplication of the short arm of chromosome 9. Analysis of five cases
-
Cuoco C, Gimelli G, Pasquali F, Poloni L, Zuffardi O, Alicata P, Battaglino G, Bernardi F, Cerone R, Cotellessa M, Ghidoni A, Motta S. 1982. Duplication of the short arm of chromosome 9. Analysis of five cases. Hum Genet 61:3-7.
-
(1982)
Hum Genet
, vol.61
, pp. 3-7
-
-
Cuoco, C.1
Gimelli, G.2
Pasquali, F.3
Poloni, L.4
Zuffardi, O.5
Alicata, P.6
Battaglino, G.7
Bernardi, F.8
Cerone, R.9
Cotellessa, M.10
Ghidoni, A.11
Motta, S.12
-
5
-
-
0018294329
-
Partial duplication of the short arm of chromosome 9 (p13 → p22) in a child with typical trisomy phenotype
-
Fryns JP, Casaer P, Van den Berghe H. 1979. Partial duplication of the short arm of chromosome 9 (p13 → p22) in a child with typical trisomy phenotype. Hum Genet 46:231-235.
-
(1979)
Hum Genet
, vol.46
, pp. 231-235
-
-
Fryns, J.P.1
Casaer, P.2
Van Den Berghe, H.3
-
6
-
-
0032557730
-
Direct duplication of 9p22 → p24 in a child with duplication 9p syndrome
-
Fujimoto A, Lin MS, Schwarts S. 1998 Direct duplication of 9p22 → p24 in a child with duplication 9p syndrome. Am J Med Genet 77:268-271.
-
(1998)
Am J Med Genet
, vol.77
, pp. 268-271
-
-
Fujimoto, A.1
Lin, M.S.2
Schwarts, S.3
-
7
-
-
0031960521
-
Chromosome specific comparative genome hybridisation determining the origin of intrachromosomal duplications
-
Griffin DK, Sanoudou D, Adamski E, MacGiffert C, O'Brien P, Wienberg J, Ferguson-Smith MA. 1998. Chromosome specific comparative genome hybridisation determining the origin of intrachromosomal duplications. J Med Genet 35:37-41.
-
(1998)
J Med Genet
, vol.35
, pp. 37-41
-
-
Griffin, D.K.1
Sanoudou, D.2
Adamski, E.3
MacGiffert, C.4
O'Brien, P.5
Wienberg, J.6
Ferguson-Smith, M.A.7
-
8
-
-
0030462577
-
Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22 → p24)
-
Haddad BR, Lin AE, Wyandt H, Milunsky A. 1996. Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22 → p24). J Med Genet 33:1045-1047.
-
(1996)
J Med Genet
, vol.33
, pp. 1045-1047
-
-
Haddad, B.R.1
Lin, A.E.2
Wyandt, H.3
Milunsky, A.4
-
9
-
-
0014994769
-
Presumed trisomy for the short arm of chromosome no 9 due to inherited translocation
-
Hoehn H, Engel W, Reinwein H. 1971. Presumed trisomy for the short arm of chromosome no 9 due to inherited translocation. Hum Genet 12:175-181.
-
(1971)
Hum Genet
, vol.12
, pp. 175-181
-
-
Hoehn, H.1
Engel, W.2
Reinwein, H.3
-
10
-
-
0016826647
-
A case of partial (9p) trisomy in a family with a balanced translocation 46, XX, t (1p+9q-)
-
Mason MK, Spencer DA, Rutter A. 1975. A case of partial (9p) trisomy in a family with a balanced translocation 46, XX, t (1p+9q-). J Med Genet 12:310-314.
-
(1975)
J Med Genet
, vol.12
, pp. 310-314
-
-
Mason, M.K.1
Spencer, D.A.2
Rutter, A.3
-
11
-
-
0028343233
-
Automated construction of genetic linkage maps using an expert system (multi map): A human genome linkage map
-
Matise TC, Perlin M, Chakravarti A. 1994. Automated construction of genetic linkage maps using an expert system (Multi Map): a human genome linkage map. Nat Genet 6:384-390.
-
(1994)
Nat Genet
, vol.6
, pp. 384-390
-
-
Matise, T.C.1
Perlin, M.2
Chakravarti, A.3
-
12
-
-
0023184034
-
Duplication 9p due to unequal sister chromatid exchange
-
Mattina T, Sorge G, Milone G, Garozzo R, Conti L. 1987. Duplication 9p due to unequal sister chromatid exchange. J Med Genet 24:303-305.
-
(1987)
J Med Genet
, vol.24
, pp. 303-305
-
-
Mattina, T.1
Sorge, G.2
Milone, G.3
Garozzo, R.4
Conti, L.5
-
13
-
-
0024284028
-
A simple salting out procedure for extracting DNA from nucleated cells
-
Miller SA, Dykes DD, Polesky HF. 1988. A simple salting out procedure for extracting DNA from nucleated cells. Nucleic Acids Res 16:1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
14
-
-
0021925619
-
De novo tandem duplication 9p (p12 → p24) with normal GALT activity in red cells
-
Motegi T, Watanabe K, Nakamura N, Hasegawa T, Yanagawa Y. 1985. De novo tandem duplication 9p (p12 → p24) with normal GALT activity in red cells. J Med Genet 22:64-66.
-
(1985)
J Med Genet
, vol.22
, pp. 64-66
-
-
Motegi, T.1
Watanabe, K.2
Nakamura, N.3
Hasegawa, T.4
Yanagawa, Y.5
-
15
-
-
0016709002
-
Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+9q-)
-
Penchaszadeh VB, Coco R. 1975. Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+9q-). J Med Genet 12:301-305.
-
(1975)
J Med Genet
, vol.12
, pp. 301-305
-
-
Penchaszadeh, V.B.1
Coco, R.2
-
16
-
-
0027242034
-
Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop
-
Phelan MC, Stevenson RE, Anderson EV. 1993. Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop. Am J Med Genet 46:304-308.
-
(1993)
Am J Med Genet
, vol.46
, pp. 304-308
-
-
Phelan, M.C.1
Stevenson, R.E.2
Anderson, E.V.3
-
17
-
-
0025425540
-
Linkage analysis of the human HMG14 gene on chromosome 21 using a GT nucleotide repeat as polymorphic marker
-
Petersen MB, Economou EP, Slangenhaupt SA, Chakravarti A, Antonarakis SE. 1990. Linkage analysis of the human HMG14 gene on chromosome 21 using a GT nucleotide repeat as polymorphic marker. Genomics 7:136-138.
-
(1990)
Genomics
, vol.7
, pp. 136-138
-
-
Petersen, M.B.1
Economou, E.P.2
Slangenhaupt, S.A.3
Chakravarti, A.4
Antonarakis, S.E.5
-
18
-
-
0026069455
-
Use of short sequence DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome
-
Petersen MB, Schintzel AA, Binkert F, Tranebiaerg L, Mikkelsen M, Collins FA, Economou EP, Antonarakis SE. 1991. Use of short sequence DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome. Am J Hum Genet 48:65-71.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 65-71
-
-
Petersen, M.B.1
Schintzel, A.A.2
Binkert, F.3
Tranebiaerg, L.4
Mikkelsen, M.5
Collins, F.A.6
Economou, E.P.7
Antonarakis, S.E.8
-
19
-
-
0026070467
-
A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescence in situ hybridization
-
Rocchi M, Archidiacono N, Ward DC, Baldini A. 1991. A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescence in situ hybridization. Genomics 9:517-523.
-
(1991)
Genomics
, vol.9
, pp. 517-523
-
-
Rocchi, M.1
Archidiacono, N.2
Ward, D.C.3
Baldini, A.4
-
20
-
-
0031905005
-
Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9) (q24.1;q34.3) and a rare constitutional VHL missense subtitution
-
Teh BT, Blennow E, Giraud S, Hii S, Sahlèn S, Brookwell R, Brauch H, Nordenskjold N, Larsson C, Nicol D. 1998. Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9) (q24.1;q34.3) and a rare constitutional VHL missense subtitution. Genes Chromosomes Cancer 21:260-264.
-
(1998)
Genes Chromosomes Cancer
, vol.21
, pp. 260-264
-
-
Teh, B.T.1
Blennow, E.2
Giraud, S.3
Hii, S.4
Sahlèn, S.5
Brookwell, R.6
Brauch, H.7
Nordenskjold, N.8
Larsson, C.9
Nicol, D.10
-
21
-
-
0021965723
-
Brief cytogenetic report on maternal translocation t (7;9) (p22;q13): Two sibs with duplication on 9p and one sib with the balanced translocation
-
Wajntal A, Gonzalez CH, Koiffmann CP, de Souza DH. 1985. Brief cytogenetic report on maternal translocation t (7;9) (p22;q13): two sibs with duplication on 9p and one sib with the balanced translocation. Am J Med Genet 20:265-269.
-
(1985)
Am J Med Genet
, vol.20
, pp. 265-269
-
-
Wajntal, A.1
Gonzalez, Ch.2
Koiffmann, C.P.3
De Souza, D.H.4
-
22
-
-
0019775002
-
9p duplication confir-med by gene dosage effect: Report of two patients
-
Zadeh TM, Funderburk SJ, Carrel R, Dumars KW. 1981. 9p duplication confir-med by gene dosage effect: report of two patients. Ann Genet 24:242-244.
-
(1981)
Ann Genet
, vol.24
, pp. 242-244
-
-
Zadeh, T.M.1
Funderburk, S.J.2
Carrel, R.3
Dumars, K.W.4
|