-
1
-
-
0029041078
-
Reproductive outcome in 3 families with a satellited chromosome 4 with review of the literature
-
Arn PH, Younie L, Russo S, Zackowski JL, Mankinen C, Estabrooks L: Reproductive outcome in 3 families with a satellited chromosome 4 with review of the literature. Am J Med Genet 57:420-424 (1995).
-
(1995)
Am J Med Genet
, vol.57
, pp. 420-424
-
-
Arn, P.H.1
Younie, L.2
Russo, S.3
Zackowski, J.L.4
Mankinen, C.5
Estabrooks, L.6
-
2
-
-
0033843813
-
Chronic myelomonocytic leukaemia in a child with constitutional partial trisomy 8 mosaicism
-
Brady AF, Waters CS, Pocha MJ, Brueton LA: Chronic myelomonocytic leukaemia in a child with constitutional partial trisomy 8 mosaicism. Clin Genet 58:142-146 (2000).
-
(2000)
Clin Genet
, vol.58
, pp. 142-146
-
-
Brady, A.F.1
Waters, C.S.2
Pocha, M.J.3
Brueton, L.A.4
-
3
-
-
0028293338
-
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: Regional assignment of a presumptive gene involved in corpus callosum development
-
Digilio MC, Giannotti A, Floridia G, Uccellatore F, Mingarelli R, Danesino C, Dallapiccola B, Zuffardi O: Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum development. J Med Genet 31:238-241 (1994).
-
(1994)
J Med Genet
, vol.31
, pp. 238-241
-
-
Digilio, M.C.1
Giannotti, A.2
Floridia, G.3
Uccellatore, F.4
Mingarelli, R.5
Danesino, C.6
Dallapiccola, B.7
Zuffardi, O.8
-
4
-
-
0015230136
-
Sur une nouvelle technique d'analyse du caryotype humain
-
Dutrillaux B, Lejeune J: Sur une nouvelle technique d'analyse du caryotype humain. C R Acad Sci [D] 272:2638-2640 (1971).
-
(1971)
C R Acad Sci [D]
, vol.272
, pp. 2638-2640
-
-
Dutrillaux, B.1
Lejeune, J.2
-
5
-
-
0032927467
-
Ectopic NORs on human chromosomes 4qter and 8q11: Rare chromosomal variants detected in two families
-
Guttenbach M, Haaf T, Steinlein C, Caesar J, Schinzel A, Schmid M: Ectopic NORs on human chromosomes 4qter and 8q11: rare chromosomal variants detected in two families. J Med Genet 36:339-342 (1999).
-
(1999)
J Med Genet
, vol.36
, pp. 339-342
-
-
Guttenbach, M.1
Haaf, T.2
Steinlein, C.3
Caesar, J.4
Schinzel, A.5
Schmid, M.6
-
6
-
-
0001339561
-
Fluorescence in situ hybridization
-
Myers RA (ed): (John Wiley & Sons, Chichester)
-
Haaf T: Fluorescence in situ hybridization, in Myers RA (ed): Encyclopedia of Analytical Chemistry, vol 1, pp 4984-5006 (John Wiley & Sons, Chichester 2000).
-
(2000)
Encyclopedia of Analytical Chemistry
, vol.1
, pp. 4984-5006
-
-
Haaf, T.1
-
7
-
-
0019325857
-
Controlled silver staining of nucleolus organizer regions with a protective colloidal developer: A one-step method
-
Howell WM, Black DA: Controlled silver staining of nucleolus organizer regions with a protective colloidal developer: a one-step method. Experientia 36:1014-1016 (1980).
-
(1980)
Experientia
, vol.36
, pp. 1014-1016
-
-
Howell, W.M.1
Black, D.A.2
-
8
-
-
0031749674
-
Trisomy 8 mosaicism: A further five cases illustrating marked clinical and cytogenetic variability
-
Jordan MA, Marques I, Rosendorff J, de Ravel TJ: Trisomy 8 mosaicism: a further five cases illustrating marked clinical and cytogenetic variability. Genet Couns 9:139-146 (1998).
-
(1998)
Genet Couns
, vol.9
, pp. 139-146
-
-
Jordan, M.A.1
Marques, I.2
Rosendorff, J.3
De Ravel, T.J.4
-
9
-
-
0023732285
-
Trisomy 8 mosaicism syndrome. Two cases demonstrating variability in phenotype
-
Kurtyka ZE, Krzywka B, Piatkowska E, Radwan M, Pietrzyk JJ: Trisomy 8 mosaicism syndrome. Two cases demonstrating variability in phenotype. Clin Pediatr 27:557-564 (1988).
-
(1988)
Clin Pediatr
, vol.27
, pp. 557-564
-
-
Kurtyka, Z.E.1
Krzywka, B.2
Piatkowska, E.3
Radwan, M.4
Pietrzyk, J.J.5
-
10
-
-
0036131872
-
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases
-
Maserati E, Aprili F, Vinante F, Locatelli F, Amendola G, Zatterale A, Milone G, Minelli A, Bernardi F, Lo Curto F, Pasquali F: Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases. Genes Chromosomes Cancer 33:93-97 (2002).
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 93-97
-
-
Maserati, E.1
Aprili, F.2
Vinante, F.3
Locatelli, F.4
Amendola, G.5
Zatterale, A.6
Milone, G.7
Minelli, A.8
Bernardi, F.9
Lo Curto, F.10
Pasquali, F.11
-
11
-
-
0030671373
-
Mosaicism in trisomy 8: Phenotype differences according to tissular repartition of normal and trisomic clones
-
Miller K, Arslan-Kirchner A, Schulze B, Dudel-Neujahr A, Morlot M, Burck U, Gerresheim F: Mosaicism in trisomy 8: phenotype differences according to tissular repartition of normal and trisomic clones. Ann Genet 40:181-184 (1997).
-
(1997)
Ann Genet
, vol.40
, pp. 181-184
-
-
Miller, K.1
Arslan-Kirchner, A.2
Schulze, B.3
Dudel-Neujahr, A.4
Morlot, M.5
Burck, U.6
Gerresheim, F.7
-
13
-
-
0026752530
-
Trisomy 8p: Unusual origin detected by fluorescence in situ hybridization
-
Moore CM, Barnum K, Kaye CI, Kagan-Hallett KS, Liang JC: Trisomy 8p: unusual origin detected by fluorescence in situ hybridization. Hum Genet 89:307-310 (1992).
-
(1992)
Hum Genet
, vol.89
, pp. 307-310
-
-
Moore, C.M.1
Barnum, K.2
Kaye, C.I.3
Kagan-Hallett, K.S.4
Liang, J.C.5
-
14
-
-
0025921769
-
Chromosome abnormalities found among 34,910 newborn children: Results from a 13-year incidence study in Århus, Denmark
-
Nielsen J, Wohlert M: Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Århus, Denmark. Hum Genet 87:81-83 (1991).
-
(1991)
Hum Genet
, vol.87
, pp. 81-83
-
-
Nielsen, J.1
Wohlert, M.2
-
15
-
-
0030950630
-
Ataxic gait and mental retardation with absence of the paternal chromosome 8 and an idic(8)(p23.3): Imprinting effect or nullisomy for distal 8p genes?
-
Piantanida M, Dellavecchia C, Floridia G, Giglio S, Hoeller H, Dordi B, Danesino C, Schinzel A, Zuffardi O: Ataxic gait and mental retardation with absence of the paternal chromosome 8 and an idic(8)(p23.3): imprinting effect or nullisomy for distal 8p genes? Hum Genet 99:766-771 (1997).
-
(1997)
Hum Genet
, vol.99
, pp. 766-771
-
-
Piantanida, M.1
Dellavecchia, C.2
Floridia, G.3
Giglio, S.4
Hoeller, H.5
Dordi, B.6
Danesino, C.7
Schinzel, A.8
Zuffardi, O.9
-
16
-
-
0018858696
-
Partial trisomy 8 mosaicism with 46,XX/46,XX,-8,+dic(8)
-
Ray M, Hunter AGW: Partial trisomy 8 mosaicism with 46,XX/46,XX,-8, +dic(8). Ann Genet 23:100-102 (1980).
-
(1980)
Ann Genet
, vol.23
, pp. 100-102
-
-
Ray, M.1
Hunter, A.G.W.2
-
17
-
-
0003827196
-
-
de Gruyter, Berlin, New York
-
nd ed, pp 342-394 (de Gruyter, Berlin, New York 2001).
-
(2001)
nd Ed.
, pp. 342-394
-
-
Schinzel, A.1
-
19
-
-
0015423706
-
A simple technique for demonstrating centromeric heterochromatin
-
Sumner AT: A simple technique for demonstrating centromeric heterochromatin. Exp Cell Res 75:304-306 (1972).
-
(1972)
Exp Cell Res
, vol.75
, pp. 304-306
-
-
Sumner, A.T.1
-
20
-
-
0034790956
-
Satellites on the terminal short arm of chromosome 12 (12ps), inherited through several generations in three families: A new variant without phenotypic effect
-
Willatt L, Green AJ, Trump D: Satellites on the terminal short arm of chromosome 12 (12ps), inherited through several generations in three families: a new variant without phenotypic effect. J Med Genet 38:723-726 (2001).
-
(2001)
J Med Genet
, vol.38
, pp. 723-726
-
-
Willatt, L.1
Green, A.J.2
Trump, D.3
-
21
-
-
0029866263
-
Distal 8p deletion (8)(p23.1): An easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation
-
Wu B-L, Schneider GH, Sabatino DE, Bozovic LZ, Cao B, Korf BR: Distal 8p deletion (8)(p23.1): An easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation. Am J Med Genet 62:77-83 (1996).
-
(1996)
Am J Med Genet
, vol.62
, pp. 77-83
-
-
Wu, B.-L.1
Schneider, G.H.2
Sabatino, D.E.3
Bozovic, L.Z.4
Cao, B.5
Korf, B.R.6
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