-
1
-
-
33645840170
-
A paternally derived inverted duplication of distal 14q with a terminal 14q deletion
-
Chen C.-P., Chern S.-R., Lin S.-P., Lin C.-C., Li Y.-C., Wang T.-H., et al. A paternally derived inverted duplication of distal 14q with a terminal 14q deletion. Am J Med Genet 2005, 139A:146-150.
-
(2005)
Am J Med Genet
, vol.139 A
, pp. 146-150
-
-
Chen, C.-P.1
Chern, S.-R.2
Lin, S.-P.3
Lin, C.-C.4
Li, Y.-C.5
Wang, T.-H.6
-
2
-
-
79953803420
-
Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization
-
Chen C.-P., Su Y.-N., Chern S.-R., Hsu C.-Y., Tsai F.-J., Wu P.-C., et al. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. Taiwan J Obstet Gynecol 2011, 50:67-73.
-
(2011)
Taiwan J Obstet Gynecol
, vol.50
, pp. 67-73
-
-
Chen, C.-P.1
Su, Y.-N.2
Chern, S.-R.3
Hsu, C.-Y.4
Tsai, F.-J.5
Wu, P.-C.6
-
3
-
-
77955710069
-
Telomere capture as a frequent mechanism for stabilization of the terminal chromosomal deletion associated with inverted duplication
-
Yu S., Graf W.D. Telomere capture as a frequent mechanism for stabilization of the terminal chromosomal deletion associated with inverted duplication. Cytogenet Genome Res 2010, 129:265-274.
-
(2010)
Cytogenet Genome Res
, vol.129
, pp. 265-274
-
-
Yu, S.1
Graf, W.D.2
-
4
-
-
79953308641
-
Molecular characterization of an atypical inv dup del 8q. Proposal of a mechanism of formation
-
Rodríguez L., Nevado J., Vallespin E., Palomares M., Golmayo L., Bonaglia M.C., et al. Molecular characterization of an atypical inv dup del 8q. Proposal of a mechanism of formation. Am J Med Genet 2011, 155A:915-919.
-
(2011)
Am J Med Genet
, vol.155 A
, pp. 915-919
-
-
Rodríguez, L.1
Nevado, J.2
Vallespin, E.3
Palomares, M.4
Golmayo, L.5
Bonaglia, M.C.6
-
5
-
-
0017043575
-
Duplication-deficiency of the short arm of chromosome 8 following artificial insemination
-
Weleber R.G., Verma R.S., Kimberling W.J., Fieger H.G., Lubs H.A. Duplication-deficiency of the short arm of chromosome 8 following artificial insemination. Ann Génét 1976, 19:241-247.
-
(1976)
Ann Génét
, vol.19
, pp. 241-247
-
-
Weleber, R.G.1
Verma, R.S.2
Kimberling, W.J.3
Fieger, H.G.4
Lubs, H.A.5
-
6
-
-
19144369894
-
The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications
-
Floridia G., Piantanida M., Minelli A., Dellavecchia C., Bonaglia C., Rossi E., et al. The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications. Am J Hum Genet 1996, 58:785-796.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 785-796
-
-
Floridia, G.1
Piantanida, M.2
Minelli, A.3
Dellavecchia, C.4
Bonaglia, C.5
Rossi, E.6
-
7
-
-
0042232610
-
Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions
-
Ballif B.C., Yu W., Shaw C.A., Kashork C.D., Shaffer L.G. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions. Hum Mol Genet 2003, 12:2153-2165.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2153-2165
-
-
Ballif, B.C.1
Yu, W.2
Shaw, C.A.3
Kashork, C.D.4
Shaffer, L.G.5
-
8
-
-
0029021347
-
Four new cases of inverted terminal duplication: a modified hypothesis of mechanism of origin
-
Hoo J.J., Chao M., Szego K., Rauer M., Echiverri S.C., Harris C. Four new cases of inverted terminal duplication: a modified hypothesis of mechanism of origin. Am J Med Genet 1995, 58:299-304.
-
(1995)
Am J Med Genet
, vol.58
, pp. 299-304
-
-
Hoo, J.J.1
Chao, M.2
Szego, K.3
Rauer, M.4
Echiverri, S.C.5
Harris, C.6
-
9
-
-
0033024393
-
Triplication of distal chromosome 10q
-
Devriendt K., Matthijs G., Holvoet M., Schoenmakers E., Fryns J.-P. Triplication of distal chromosome 10q. J Med Genet 1999, 36:242-245.
-
(1999)
J Med Genet
, vol.36
, pp. 242-245
-
-
Devriendt, K.1
Matthijs, G.2
Holvoet, M.3
Schoenmakers, E.4
Fryns, J.-P.5
-
10
-
-
0035083784
-
Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter)
-
Petek E., Köstl G., Rauter L., Mutz I., Wagner K., Kroisel P.M. Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter). Clin Dysmorphol 2001, 10:151-153.
-
(2001)
Clin Dysmorphol
, vol.10
, pp. 151-153
-
-
Petek, E.1
Köstl, G.2
Rauter, L.3
Mutz, I.4
Wagner, K.5
Kroisel, P.M.6
-
11
-
-
0036109696
-
Distal trisomy of 10q: report of a new case of duplication 10q25.2-25.3→qter defined by FISH
-
Migliori M.V., Ciaschini A.M., Discepoli G., Abbasciano V., Barbato M., Pannone E. Distal trisomy of 10q: report of a new case of duplication 10q25.2-25.3→qter defined by FISH. Ann Génét 2002, 45:9-12.
-
(2002)
Ann Génét
, vol.45
, pp. 9-12
-
-
Migliori, M.V.1
Ciaschini, A.M.2
Discepoli, G.3
Abbasciano, V.4
Barbato, M.5
Pannone, E.6
-
12
-
-
0038242497
-
Comparative genomic hybridization-assisted prenatal diagnosis of a de novo inverted duplication of chromosome 10q. A case report
-
Chen C.-K., Chang S.-D., Chen Y.-J., Hsueh D.-W., Soong Y.-K. Comparative genomic hybridization-assisted prenatal diagnosis of a de novo inverted duplication of chromosome 10q. A case report. J Reprod Med 2003, 48:391-394.
-
(2003)
J Reprod Med
, vol.48
, pp. 391-394
-
-
Chen, C.-K.1
Chang, S.-D.2
Chen, Y.-J.3
Hsueh, D.-W.4
Soong, Y.-K.5
-
13
-
-
2342472763
-
Chromosomal 10q26 trisomy resulting from paternal t(9;10) (pter;q26.1)
-
Hou J.-W. Chromosomal 10q26 trisomy resulting from paternal t(9;10) (pter;q26.1). J Formos Med Assoc 2003, 102:887-892.
-
(2003)
J Formos Med Assoc
, vol.102
, pp. 887-892
-
-
Hou, J.-W.1
-
14
-
-
77953544493
-
Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1-q26.3
-
Carter M.T., Dyack S., Richer J. Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1-q26.3. Clin Dysmorphol 2010, 19:140-145.
-
(2010)
Clin Dysmorphol
, vol.19
, pp. 140-145
-
-
Carter, M.T.1
Dyack, S.2
Richer, J.3
-
15
-
-
78650665028
-
Two concurrent chromosomal aberrations involving interstitial deletion in 1q24.2q25.2 and inverted duplication and deletion in 10q26 in a patient with stroke associated with antithrombin deficiency and a patent foramen ovale
-
Kibe T., Mori Y., Okanishi T., Shimojima K., Yokochi K., Yamamoto T. Two concurrent chromosomal aberrations involving interstitial deletion in 1q24.2q25.2 and inverted duplication and deletion in 10q26 in a patient with stroke associated with antithrombin deficiency and a patent foramen ovale. Am J Med Genet 2011, 155A:215-220.
-
(2011)
Am J Med Genet
, vol.155 A
, pp. 215-220
-
-
Kibe, T.1
Mori, Y.2
Okanishi, T.3
Shimojima, K.4
Yokochi, K.5
Yamamoto, T.6
-
16
-
-
78650736849
-
Balanced reciprocal translocations detected at amniocentesis
-
Chen C.-P., Wu P.-C., Su Y.-N., Chern S.-R., Tsai F.-J., Lee C.-C., et al. Balanced reciprocal translocations detected at amniocentesis. Taiwan J Obstet Gynecol 2010, 49:455-467.
-
(2010)
Taiwan J Obstet Gynecol
, vol.49
, pp. 455-467
-
-
Chen, C.-P.1
Wu, P.-C.2
Su, Y.-N.3
Chern, S.-R.4
Tsai, F.-J.5
Lee, C.-C.6
-
17
-
-
79953783581
-
Unbalanced reciprocal translocations at amniocentesis
-
Chen C.-P., Wu P.-C., Lin C.-J., Chern S.-R., Tsai F.-J., Lee C.-C., et al. Unbalanced reciprocal translocations at amniocentesis. Taiwan J Obstet Gynecol 2011, 50:48-57.
-
(2011)
Taiwan J Obstet Gynecol
, vol.50
, pp. 48-57
-
-
Chen, C.-P.1
Wu, P.-C.2
Lin, C.-J.3
Chern, S.-R.4
Tsai, F.-J.5
Lee, C.-C.6
-
18
-
-
78650746993
-
Partial trisomy 10q (10q25.1→qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization
-
Chen C.-P., Su Y.-N., Tsai F.-J., Chern S.-R., Hsu C.-Y., Wu P.-C., et al. Partial trisomy 10q (10q25.1→qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization. Taiwan J Obstet Gynecol 2010, 49:539-543.
-
(2010)
Taiwan J Obstet Gynecol
, vol.49
, pp. 539-543
-
-
Chen, C.-P.1
Su, Y.-N.2
Tsai, F.-J.3
Chern, S.-R.4
Hsu, C.-Y.5
Wu, P.-C.6
-
19
-
-
0242426672
-
Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases
-
Irving M., Hanson H., Turnpenny P., Brewer C., Ogilvie C.M., Davies A., et al. Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases. Am J Med Genet 2003, 123A:153-163.
-
(2003)
Am J Med Genet
, vol.123 A
, pp. 153-163
-
-
Irving, M.1
Hanson, H.2
Turnpenny, P.3
Brewer, C.4
Ogilvie, C.M.5
Davies, A.6
-
20
-
-
21844463593
-
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3→qter) and partial trisomy 18q (18q23→qter) in a fetus associated with cystic hygroma and ambiguous genitalia
-
Chen C.-P., Chern S.-R., Wang T.-H., Hsueh D.-W., Lee C.-C., Town D.-D., et al. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3→qter) and partial trisomy 18q (18q23→qter) in a fetus associated with cystic hygroma and ambiguous genitalia. Prenat Diagn 2005, 25:492-496.
-
(2005)
Prenat Diagn
, vol.25
, pp. 492-496
-
-
Chen, C.-P.1
Chern, S.-R.2
Wang, T.-H.3
Hsueh, D.-W.4
Lee, C.-C.5
Town, D.-D.6
|