-
2
-
-
9344249807
-
Mosaicism for trisomy 13 with 13/13 translocation and balanced 13/21 translocation in a patient with 13p
-
Anderson CE, Shulkin JD, Mohandas T. 1979. Mosaicism for trisomy 13 with 13/13 translocation and balanced 13/21 translocation in a patient with 13p. Am J Hum Genet 31: 87A.
-
(1979)
Am J Hum Genet
, vol.31
-
-
Anderson, C.E.1
Shulkin, J.D.2
Mohandas, T.3
-
3
-
-
28544433719
-
Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings
-
Aslan H, Karaman B, Yildirim G, Ceylan Y. 2005. Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings. Prenat Diagn 25: 1024-1027.
-
(2005)
Prenat Diagn
, vol.25
, pp. 1024-1027
-
-
Aslan, H.1
Karaman, B.2
Yildirim, G.3
Ceylan, Y.4
-
4
-
-
0016309101
-
Down's syndrome associated with two Robertsonian translocations, 45,XX,-15,-21,+t(15q;21q) and 46,XX,-21,+t(21q;21q)
-
Atkins L, Bartsocas CS. 1974. Down's syndrome associated with two Robertsonian translocations, 45, XX, -15, -21, +t(15q;21q) and 46, XX, -21, +t(21q;21q). J Med Genet 11: 306-309.
-
(1974)
J Med Genet
, vol.11
, pp. 306-309
-
-
Atkins, L.1
Bartsocas, C.S.2
-
5
-
-
0037438672
-
Mosaicism in a patient with Down syndrome reveals post-fertilization formation of a Robertsonian translocation and isochromosome
-
Bandyopadhyay R, McCaskill C, Knox-Du Bois C, Zhou Y, Berend SA, Bijlsma E, Shaffer LG. 2003. Mosaicism in a patient with Down syndrome reveals post-fertilization formation of a Robertsonian translocation and isochromosome. Am J Med Genet Part A 116A: 159-163.
-
(2003)
Am J Med Genet Part A
, vol.116
, pp. 159-163
-
-
Bandyopadhyay, R.1
McCaskill, C.2
Knox-Du Bois, C.3
Zhou, Y.4
Berend, S.A.5
Bijlsma, E.6
Shaffer, L.G.7
-
6
-
-
0031755758
-
Molecular analysis of mosaicism for two different de novo acrocentric rearrangements demonstrates diversity in Robertsonian translocation formation
-
Berend SA, Canun S, McCaskill C, Page SL, Shaffer LG. 1998. Molecular analysis of mosaicism for two different de novo acrocentric rearrangements demonstrates diversity in Robertsonian translocation formation. Am J Med Genet 80: 252-259.
-
(1998)
Am J Med Genet
, vol.80
, pp. 252-259
-
-
Berend, S.A.1
Canun, S.2
McCaskill, C.3
Page, S.L.4
Shaffer, L.G.5
-
10
-
-
71949105699
-
Rare rearrangements: A "jumping satellite" in one family and autosomal location of the SRY gene in an XX male
-
Chien SC, Li YC, Ho M, Hsu PC, Teng RH, Lin WD, Tsai FJ, Lin CC. 2009. Rare rearrangements: A "jumping satellite" in one family and autosomal location of the SRY gene in an XX male. Am J Med Genet Part A 149A: 2775-2781.
-
(2009)
Am J Med Genet Part A
, vol.149
, pp. 2775-2781
-
-
Chien, S.C.1
Li, Y.C.2
Ho, M.3
Hsu, P.C.4
Teng, R.H.5
Lin, W.D.6
Tsai, F.J.7
Lin, C.C.8
-
11
-
-
0024559975
-
An unusual case of mosaic Down's syndrome involving two different Robertsonian translocations
-
Clarke MJ, Thomson DAG, Griffiths MJ, Bissenden JG, Aukett A, Watt JL. 1989. An unusual case of mosaic Down's syndrome involving two different Robertsonian translocations. J Med Genet 26: 198-201.
-
(1989)
J Med Genet
, vol.26
, pp. 198-201
-
-
Clarke, M.J.1
Thomson, D.A.G.2
Griffiths, M.J.3
Bissenden, J.G.4
Aukett, A.5
Watt, J.L.6
-
12
-
-
0018952074
-
Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family
-
De Pina Neto JM, Ferrari I. 1980. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family. Am J Med Genet 5: 25-33.
-
(1980)
Am J Med Genet
, vol.5
, pp. 25-33
-
-
De Pina Neto, J.M.1
Ferrari, I.2
-
13
-
-
16944363754
-
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome
-
Devriendt K, Petit P, Matthijs G, Vermeesch JR, Holvoet M, Muelenaere AD, Marynen P, Cassiman JJ, Fryns JP. 1997. Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome. J Med Genet 34: 395-399.
-
(1997)
J Med Genet
, vol.34
, pp. 395-399
-
-
Devriendt, K.1
Petit, P.2
Matthijs, G.3
Vermeesch, J.R.4
Holvoet, M.5
Muelenaere, A.D.6
Marynen, P.7
Cassiman, J.J.8
Fryns, J.P.9
-
14
-
-
0007544477
-
Unbalanced, unstable translocations of 22q
-
Drake VJ, Tunnell S, Ward BE, Robinson A. 1985. Unbalanced, unstable translocations of 22q. Am J Hum Genet 37S: A91.
-
(1985)
Am J Hum Genet
, vol.37
-
-
Drake, V.J.1
Tunnell, S.2
Ward, B.E.3
Robinson, A.4
-
16
-
-
49949118702
-
Prenatal diagnosis of monosomy 18p involving a jumping translocation
-
Edwards S, Waters JJ. 2008. Prenatal diagnosis of monosomy 18p involving a jumping translocation. Prenat Diagn 28: 764-766.
-
(2008)
Prenat Diagn
, vol.28
, pp. 764-766
-
-
Edwards, S.1
Waters, J.J.2
-
17
-
-
0027260825
-
Moving satellites and unstable chromosome translocations: Clinical and cytogenetic implications
-
Farrell SA, Winsor EJ, Markovic VD. 1993. Moving satellites and unstable chromosome translocations: Clinical and cytogenetic implications. Am J Med Genet 46: 715-720.
-
(1993)
Am J Med Genet
, vol.46
, pp. 715-720
-
-
Farrell, S.A.1
Winsor, E.J.2
Markovic, V.D.3
-
18
-
-
0017191785
-
"Jumping" satellites in three generations: A warning for paternity tests and prenatal diagnosis
-
Gimelli G, Porro E, Santi F, Scappaticci S, Zuffardi O. 1976. "Jumping" satellites in three generations: A warning for paternity tests and prenatal diagnosis. Hum Genet 34: 315-318.
-
(1976)
Hum Genet
, vol.34
, pp. 315-318
-
-
Gimelli, G.1
Porro, E.2
Santi, F.3
Scappaticci, S.4
Zuffardi, O.5
-
19
-
-
0030752632
-
Fluorescence in situ hybridization assessment of the telomeric regions of jumping translocations in a case of aggressive B-cell non-Hodgkin lymphoma
-
Gray BA, Bent-Williams A, Wadsworth J, Maiese RL, Bhatia A, Zori RT. 1997. Fluorescence in situ hybridization assessment of the telomeric regions of jumping translocations in a case of aggressive B-cell non-Hodgkin lymphoma. Cancer Genet Cytogenet 98: 20-27.
-
(1997)
Cancer Genet Cytogenet
, vol.98
, pp. 20-27
-
-
Gray, B.A.1
Bent-Williams, A.2
Wadsworth, J.3
Maiese, R.L.4
Bhatia, A.5
Zori, R.T.6
-
20
-
-
0023637460
-
Neonatal diagnosis of Prader-Willi syndrome and its implications
-
Greenberg F, Elder FFB, Ledbetter DH. 1987. Neonatal diagnosis of Prader-Willi syndrome and its implications. Am J Med Genet 28: 845-856.
-
(1987)
Am J Med Genet
, vol.28
, pp. 845-856
-
-
Greenberg, F.1
Elder, F.F.B.2
Ledbetter, D.H.3
-
21
-
-
0029763259
-
A jumping Robertsonian translocation: A molecular and cytogenetic study
-
Gross SJ, Tharapel AT, Phillips OP, Shulman LP, Pivnick EK, Park VM. 1996. A jumping Robertsonian translocation: A molecular and cytogenetic study. Hum Genet 98: 291-296.
-
(1996)
Hum Genet
, vol.98
, pp. 291-296
-
-
Gross, S.J.1
Tharapel, A.T.2
Phillips, O.P.3
Shulman, L.P.4
Pivnick, E.K.5
Park, V.M.6
-
22
-
-
0030986393
-
Accuracy of cytogenetic findings on chorionic villus sampling (CVS)-Diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centers contributing to EUCROMIC 1986-1992
-
Hahnemann JM, Vejerslev LO. 1997. Accuracy of cytogenetic findings on chorionic villus sampling (CVS)-Diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centers contributing to EUCROMIC 1986-1992. Prenat Diagn 17: 801-820.
-
(1997)
Prenat Diagn
, vol.17
, pp. 801-820
-
-
Hahnemann, J.M.1
Vejerslev, L.O.2
-
23
-
-
0032032299
-
Shortened telomeres involved in a case with a jumping translocation at 1q21
-
Hatakeyama S, Fujita K, Mori H, Omine M, Ishikawa F. 1998. Shortened telomeres involved in a case with a jumping translocation at 1q21. Blood 91: 1514-1519.
-
(1998)
Blood
, vol.91
, pp. 1514-1519
-
-
Hatakeyama, S.1
Fujita, K.2
Mori, H.3
Omine, M.4
Ishikawa, F.5
-
24
-
-
0026776170
-
Jumping translocations originate clonal rearrangements in SV40-transformed human fibroblasts
-
Hoffschir F, Ricoul M, Lemieux N, Estrade S, Cassingena R, Dutrillaux B. 1992. Jumping translocations originate clonal rearrangements in SV40-transformed human fibroblasts. Int J Cancer 52: 130-136.
-
(1992)
Int J Cancer
, vol.52
, pp. 130-136
-
-
Hoffschir, F.1
Ricoul, M.2
Lemieux, N.3
Estrade, S.4
Cassingena, R.5
Dutrillaux, B.6
-
25
-
-
33544459968
-
"Jumping translocation" involving 21p in amniocytes
-
Hulley BJ, Bleigh CB, McAdoo SL, Boyd BK, Wenger SL. 2003. "Jumping translocation" involving 21p in amniocytes. J Assoc Genet Technol 29: 91.
-
(2003)
J Assoc Genet Technol
, vol.29
, pp. 91
-
-
Hulley, B.J.1
Bleigh, C.B.2
McAdoo, S.L.3
Boyd, B.K.4
Wenger, S.L.5
-
26
-
-
68049093005
-
Jumping translocation in a phenotypically normal male: A study of mosaicism in spermatozoa, lymphocytes, and fibroblasts
-
Iwarsson E, Sahlén S, Nordgren A. 2009. Jumping translocation in a phenotypically normal male: A study of mosaicism in spermatozoa, lymphocytes, and fibroblasts. Am J Med Genet Part A 149A: 1706-1711.
-
(2009)
Am J Med Genet Part A
, vol.149
, pp. 1706-1711
-
-
Iwarsson, E.1
Sahlén, S.2
Nordgren, A.3
-
27
-
-
0016187952
-
A family with two translocations and a polymorphism involving chromosome 14
-
Jacobs PA, Buckton KE, Christie S, Newton M, Matthew D. 1974. A family with two translocations and a polymorphism involving chromosome 14. J Med Genet 11: 65-68.
-
(1974)
J Med Genet
, vol.11
, pp. 65-68
-
-
Jacobs, P.A.1
Buckton, K.E.2
Christie, S.3
Newton, M.4
Matthew, D.5
-
28
-
-
0031798360
-
Jumping translocation with partial duplications and triplications of chromosomes 7 and 15
-
Jewett T, Marnane D, Stewart W, Hayworth-Hodge R, Finklea L, Klinepeter K, Rao PN, Pettenati MJ. 1998. Jumping translocation with partial duplications and triplications of chromosomes 7 and 15. Clin Genet 53: 415-420.
-
(1998)
Clin Genet
, vol.53
, pp. 415-420
-
-
Jewett, T.1
Marnane, D.2
Stewart, W.3
Hayworth-Hodge, R.4
Finklea, L.5
Klinepeter, K.6
Rao, P.N.7
Pettenati, M.J.8
-
29
-
-
0029007111
-
Non-random jumping translocations as a result of SV40 large T-antigen expression in benign human tumor cells
-
Kazmierczak B, Stern C, Bartnitzke S, Bullerdiek J. 1995. Non-random jumping translocations as a result of SV40 large T-antigen expression in benign human tumor cells. Cell Biol Int 19: 315-322.
-
(1995)
Cell Biol Int
, vol.19
, pp. 315-322
-
-
Kazmierczak, B.1
Stern, C.2
Bartnitzke, S.3
Bullerdiek, J.4
-
31
-
-
0007503338
-
A partially deleted #22 translocated to a #12 and a #19 in a newborn
-
Ketterer DM, Casey J, Word A, Sawalqah H, Giles HR. 1984. A partially deleted #22 translocated to a #12 and a #19 in a newborn. Am J Hum Genet 36S: A99.
-
(1984)
Am J Hum Genet
, vol.36
-
-
Ketterer, D.M.1
Casey, J.2
Word, A.3
Sawalqah, H.4
Giles, H.R.5
-
33
-
-
0035132915
-
Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation
-
Lefort G, Blanchet P, Chaze AM, Girardet A, Sarda P, Demaille J, Pellestor F. 2001. Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation. J Med Genet 38: 67-73.
-
(2001)
J Med Genet
, vol.38
, pp. 67-73
-
-
Lefort, G.1
Blanchet, P.2
Chaze, A.M.3
Girardet, A.4
Sarda, P.5
Demaille, J.6
Pellestor, F.7
-
34
-
-
0018568073
-
Translocation sauteuse (5p;15q), (8q;15q), (12q;15q)
-
Lejeune J, Maunoury C, Prieur M, Van den Akker J. 1979. Translocation sauteuse (5p;15q), (8q;15q), (12q;15q). Ann Genet 22: 210-213.
-
(1979)
Ann Genet
, vol.22
, pp. 210-213
-
-
Lejeune, J.1
Maunoury, C.2
Prieur, M.3
Van den Akker, J.4
-
36
-
-
0019976740
-
Two Robertsonian translocations in a boy with mental retardation
-
Lieber E, Shah P. 1982. Two Robertsonian translocations in a boy with mental retardation. J Med Genet 19: 229-232.
-
(1982)
J Med Genet
, vol.19
, pp. 229-232
-
-
Lieber, E.1
Shah, P.2
-
37
-
-
0024347093
-
A case of de novo i(12p)with 12q whole-arm translocation mosaicism
-
Marques-de-Faria AP, Hackel C. 1989. A case of de novo i(12p)with 12q whole-arm translocation mosaicism. Am J Med Genet 32: 453-456.
-
(1989)
Am J Med Genet
, vol.32
, pp. 453-456
-
-
Marques-de-Faria, A.P.1
Hackel, C.2
-
38
-
-
0025967488
-
Unstable translocations: A new case?
-
Mattina T, Milana G, D'Agata A, Conti L, Sciacca F. 1991. Unstable translocations: A new case? Clin Genet 39: 149-510.
-
(1991)
Clin Genet
, vol.39
, pp. 149-510
-
-
Mattina, T.1
Milana, G.2
D'Agata, A.3
Conti, L.4
Sciacca, F.5
-
39
-
-
0026771543
-
The presence of interstitial telomeric sequences in constitutional chromosome abnormalities
-
Park VM, Gustashaw KM, Wathen TM. 1992. The presence of interstitial telomeric sequences in constitutional chromosome abnormalities. Am J Hum Genet 50: 914-923.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 914-923
-
-
Park, V.M.1
Gustashaw, K.M.2
Wathen, T.M.3
-
40
-
-
0031923651
-
Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation
-
Petit P, Devriendt K, Vermeesch JR, de Cock P, Fryns JP. 1998. Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation. Ann Genet 41: 22-26.
-
(1998)
Ann Genet
, vol.41
, pp. 22-26
-
-
Petit, P.1
Devriendt, K.2
Vermeesch, J.R.3
de Cock, P.4
Fryns, J.P.5
-
41
-
-
0033772181
-
Fusion of 9 beta-satellite and telomere (TTAGGG)n sequences results in a jumping translocation
-
Reddy KS, Murphy T. 2000. Fusion of 9 beta-satellite and telomere (TTAGGG)n sequences results in a jumping translocation. Hum Genet 107: 268-275. Review.
-
(2000)
Hum Genet
, vol.107
, pp. 268-275
-
-
Reddy, K.S.1
Murphy, T.2
-
42
-
-
0032991850
-
Jumping translocations involving chromosome 1q in a patient with Crohn disease and acute monocytic leukemia: A review of the literature on jumping translocations in hematological malignancies and Crohn disease
-
Reddy KS, Parsons L, Colman L. 1999. Jumping translocations involving chromosome 1q in a patient with Crohn disease and acute monocytic leukemia: A review of the literature on jumping translocations in hematological malignancies and Crohn disease. Cancer Genet Cytogenet 109: 144-149. Review.
-
(1999)
Cancer Genet Cytogenet
, vol.109
, pp. 144-149
-
-
Reddy, K.S.1
Parsons, L.2
Colman, L.3
-
43
-
-
0024999897
-
Nonreciprocal and jumping translocations of 15q11qter in Prader-Willi syndrome
-
Rivera H, Zuffardi O, Gargantini L. 1990. Nonreciprocal and jumping translocations of 15q11qter in Prader-Willi syndrome. Am J Med Genet 37: 311-317.
-
(1990)
Am J Med Genet
, vol.37
, pp. 311-317
-
-
Rivera, H.1
Zuffardi, O.2
Gargantini, L.3
-
44
-
-
0027527239
-
Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences
-
Rossi E, Floridia G, Casali M, Danesino C, Chiumello G, Bernardi F, Magnani I, Papi L, Mura M, Zuffardi O. 1993. Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences. J Med Genet 30: 926-931.
-
(1993)
J Med Genet
, vol.30
, pp. 926-931
-
-
Rossi, E.1
Floridia, G.2
Casali, M.3
Danesino, C.4
Chiumello, G.5
Bernardi, F.6
Magnani, I.7
Papi, L.8
Mura, M.9
Zuffardi, O.10
-
45
-
-
0036674397
-
Interstitial telomeres of an inv(9)(p11.2;q34) involved in a jumping translocation found in a woman through a stable unbalanced translocation in her malformed child
-
Sala E, Villa N, Riva P, Varisco T, Larizza L, Dalprà L. 2002. Interstitial telomeres of an inv(9)(p11.2;q34) involved in a jumping translocation found in a woman through a stable unbalanced translocation in her malformed child. J Med Genet 39: e42.
-
(2002)
J Med Genet
, vol.39
-
-
Sala, E.1
Villa, N.2
Riva, P.3
Varisco, T.4
Larizza, L.5
Dalprà, L.6
-
46
-
-
0032030675
-
Jumping translocations of chromosome 1q in multiple myeloma: Evidence for a mechanism involving decondensation of pericentromeric heterochromatin
-
Sawyer JR, Tricot G, Mattox S, Jagannath S, Barlogie B. 1998. Jumping translocations of chromosome 1q in multiple myeloma: Evidence for a mechanism involving decondensation of pericentromeric heterochromatin. Blood 91: 1732-1741.
-
(1998)
Blood
, vol.91
, pp. 1732-1741
-
-
Sawyer, J.R.1
Tricot, G.2
Mattox, S.3
Jagannath, S.4
Barlogie, B.5
-
47
-
-
0023720796
-
Unstable translocation t(14;21) in a man, inherited as a t(13;14) in one of his daughters
-
Siffroi JP, Viguie F, Romani F. 1988. Unstable translocation t(14;21) in a man, inherited as a t(13;14) in one of his daughters. Clin Genet 34: 15-19.
-
(1988)
Clin Genet
, vol.34
, pp. 15-19
-
-
Siffroi, J.P.1
Viguie, F.2
Romani, F.3
-
48
-
-
0344586770
-
The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3
-
Stankiewicz P, Cheung SW, Shaw CJ, Saleki R, Szigeti K, Lupski JR. 2003. The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3. Cytogenet Genome Res 101: 118-123.
-
(2003)
Cytogenet Genome Res
, vol.101
, pp. 118-123
-
-
Stankiewicz, P.1
Cheung, S.W.2
Shaw, C.J.3
Saleki, R.4
Szigeti, K.5
Lupski, J.R.6
-
49
-
-
0021130616
-
Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement
-
Tharapel AT, Redheendran R, Mankinen CB, Kukolich MK. 1984. Mosaic Down's syndrome with de novo 45, XX, -21, -22, +t(21q;22q)/46, XX, -21, +t(21q;21q) rearrangement. J Med Genet 21: 391-395.
-
(1984)
J Med Genet
, vol.21
, pp. 391-395
-
-
Tharapel, A.T.1
Redheendran, R.2
Mankinen, C.B.3
Kukolich, M.K.4
-
50
-
-
0019406235
-
Unstable familial translocations: A t(11;22)mat inherited as a t(11;15)
-
Tomkins DJ. 1981. Unstable familial translocations: A t(11;22)mat inherited as a t(11;15). Am J Hum Genet 33: 745-751.
-
(1981)
Am J Hum Genet
, vol.33
, pp. 745-751
-
-
Tomkins, D.J.1
-
51
-
-
0031006263
-
Interstitial telomeric sequences at the junction site of a jumping translocation
-
Vermeesch JR, Petit P, Speleman F, Devriendt K, Fryns JP, Marynen P. 1997. Interstitial telomeric sequences at the junction site of a jumping translocation. Hum Genet 99: 735-737.
-
(1997)
Hum Genet
, vol.99
, pp. 735-737
-
-
Vermeesch, J.R.1
Petit, P.2
Speleman, F.3
Devriendt, K.4
Fryns, J.P.5
Marynen, P.6
-
52
-
-
0017881582
-
Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q)
-
Vianna-Morgante AM, Nunesmaia HG. 1978. Dissociation as probable origin of mosaic 45, XY, t(15;21)/46, XY, i(21q). J Med Genet 15: 305-310.
-
(1978)
J Med Genet
, vol.15
, pp. 305-310
-
-
Vianna-Morgante, A.M.1
Nunesmaia, H.G.2
-
53
-
-
0029963913
-
Jumping translocation in a phenotypically normal female
-
Von Ballestrem CL, Boavida MG, Zuther C, Carreiro MH, David D, Gal A, Schwinger E. 1996. Jumping translocation in a phenotypically normal female. Clin Genet 49: 156-159.
-
(1996)
Clin Genet
, vol.49
, pp. 156-159
-
-
Von Ballestrem, C.L.1
Boavida, M.G.2
Zuther, C.3
Carreiro, M.H.4
David, D.5
Gal, A.6
Schwinger, E.7
-
54
-
-
0344795535
-
Jumping translocations of 9q onto 14p, 13q and 7q, and pseudoisochromosome 9p trisomy syndrome
-
Wakui K, Hidaka E, Ishikawa M, Ishikawa M, Katsuyama T, Fukushima Y. 2000. Jumping translocations of 9q onto 14p, 13q and 7q, and pseudoisochromosome 9p trisomy syndrome. Am J Hum Gen Suppl 167: 152.
-
(2000)
Am J Hum Gen Suppl
, vol.167
, pp. 152
-
-
Wakui, K.1
Hidaka, E.2
Ishikawa, M.3
Ishikawa, M.4
Katsuyama, T.5
Fukushima, Y.6
-
55
-
-
3843134061
-
Pathogenesis of jumping translocations: A molecular cytogenetics study
-
Wan TS, Ma SK, Chow EY, Li YH, Lin SY, Chan LC. 2004. Pathogenesis of jumping translocations: A molecular cytogenetics study. Leukemia Res 28: 1074-1079.
-
(2004)
Leukemia Res
, vol.28
, pp. 1074-1079
-
-
Wan, T.S.1
Ma, S.K.2
Chow, E.Y.3
Li, Y.H.4
Lin, S.Y.5
Chan, L.C.6
-
56
-
-
3343007090
-
Ring chromosome 18q and jumping translocation 18p in an adult male with hypergonadotrophic hypogonadism
-
Zahed L, Oreibi G, Azar C, Salti I. 2004. Ring chromosome 18q and jumping translocation 18p in an adult male with hypergonadotrophic hypogonadism. Am J Med Genet Part A 129A: 25-28.
-
(2004)
Am J Med Genet Part A
, vol.129
, pp. 25-28
-
-
Zahed, L.1
Oreibi, G.2
Azar, C.3
Salti, I.4
-
57
-
-
0007498946
-
Familial mosicism attributable to a new gene
-
Zellweger H, Abbo G. 1965. Familial mosicism attributable to a new gene. Lancet 1: 455-457.
-
(1965)
Lancet
, vol.1
, pp. 455-457
-
-
Zellweger, H.1
Abbo, G.2
|