-
1
-
-
0009650560
-
A Phenotypic Female with 49 Chromosomes, Presumably XXXXX. a Case Report
-
10.1016/S0022-3476(63)80190-0. 14089814
-
A Phenotypic Female with 49 Chromosomes, Presumably XXXXX. a Case Report. N Kesaree PV Woolley Jr, J Pediatr 1963 63 1099 1103 10.1016/S0022-3476(63) 80190-0 14089814
-
(1963)
J Pediatr
, vol.63
, pp. 1099-1103
-
-
Kesaree, N.1
-
2
-
-
0014378164
-
48,XXXX-49,XXXXX mosaic: Asynchronies among the late-replicating X chromosomes
-
10.1159/000129989. 5722744
-
48,XXXX-49,XXXXX mosaic: asynchronies among the late-replicating X chromosomes. N Ricci B Dallapiccola B Ventimiglia L Tiepolo M Fraccaro, Cytogenetics 1968 7 249 259 10.1159/000129989 5722744
-
(1968)
Cytogenetics
, vol.7
, pp. 249-259
-
-
Ricci, N.1
Dallapiccola, B.2
Ventimiglia, B.3
Tiepolo, L.4
Fraccaro, M.5
-
4
-
-
0015009041
-
The 49,XXXXX chromosome constitution: Similarities to the 49,XXXXY condition
-
10.1016/S0022-3476(71)80013-6. 5539772
-
The 49,XXXXX chromosome constitution: similarities to the 49,XXXXY condition. F Sergovich C Uilenberg J Pozsonyi, J Pediatr 1971 78 285 290 10.1016/S0022-3476(71)80013-6 5539772
-
(1971)
J Pediatr
, vol.78
, pp. 285-290
-
-
Sergovich, F.1
Uilenberg, C.2
Pozsonyi, J.3
-
5
-
-
0015101029
-
Penta X (49,XXXXX) chromosome constitution: A case report
-
5166615
-
Penta X (49,XXXXX) chromosome constitution: a case report. Y Yamada S Neriishi, Jinrui Idengaku Zasshi 1971 16 15 21 5166615
-
(1971)
Jinrui Idengaku Zasshi
, vol.16
, pp. 15-21
-
-
Yamada, Y.1
Neriishi, S.2
-
6
-
-
0015354113
-
Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism
-
10.1136/jmg.9.2.235. 5046636
-
Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism. P Cooke JA Black DJ Curtis, J Med Genet 1972 9 235 238 10.1136/jmg.9.2.235 5046636
-
(1972)
J Med Genet
, vol.9
, pp. 235-238
-
-
Cooke, P.1
Black, J.A.2
Curtis, D.J.3
-
7
-
-
0015355749
-
49, XXXXX syndrome in a 5-year-old girl
-
4537723
-
49, XXXXX syndrome in a 5-year-old girl. L Larget-Piet J Rivron P Baillif J Dugay I Emerit A Larget-Piet J Berthelot, Ann Genet 1972 15 115 119 4537723
-
(1972)
Ann Genet
, vol.15
, pp. 115-119
-
-
Larget-Piet, L.1
Rivron, J.2
Baillif, P.3
Dugay, J.4
Emerit, I.5
Larget-Piet, A.6
Berthelot, J.7
-
8
-
-
0016614973
-
49, XXXXX chromosome equipment in a girl with psychophysical underdevelopment
-
1221299
-
49, XXXXX chromosome equipment in a girl with psychophysical underdevelopment. ML Giovannucci-Uzielli F Torricelli Q Salvatori I Consumi GP Donzelli S Seminara, Minerva Pediatr 1975 27 2220 2229 1221299
-
(1975)
Minerva Pediatr
, vol.27
, pp. 2220-2229
-
-
Giovannucci-Uzielli, M.L.1
Torricelli, F.2
Salvatori, Q.3
Consumi, I.4
Donzelli, G.P.5
Seminara, S.6
-
10
-
-
0017826081
-
Mitotic cycles in human cell strains with sex chromosomes aneuploidy
-
10.1007/BF00283635. 669701
-
Mitotic cycles in human cell strains with sex chromosomes aneuploidy. VI Kukharenko KN Grinberg AM Kuliev, Hum Genet 1978 42 157 162 10.1007/BF00283635 669701
-
(1978)
Hum Genet
, vol.42
, pp. 157-162
-
-
Kukharenko, V.I.1
Grinberg, K.N.2
Kuliev, A.M.3
-
12
-
-
0018450102
-
The penta X (49,XXXXX) syndrome: Danger of confusing phenotype with mongolism
-
154838
-
The penta X (49,XXXXX) syndrome: danger of confusing phenotype with mongolism. DG Carpenter JM Connolly CH Carter KS Kanarek, Am J Dis Child 1979 133 330 154838
-
(1979)
Am J Dis Child
, vol.133
, pp. 330
-
-
Carpenter, D.G.1
Connolly, J.M.2
Carter, C.H.3
Kanarek, K.S.4
-
13
-
-
0018643555
-
Pentasomy X with multiple dislocations
-
10.1002/ajmg.1320040402. 539601
-
Pentasomy X with multiple dislocations. RF Dryer SR Patil HU Zellweger JM Simpson JW Hanson C Aschenbrenner SL Weinstein, Am J Med Genet 1979 4 313 321 10.1002/ajmg.1320040402 539601
-
(1979)
Am J Med Genet
, vol.4
, pp. 313-321
-
-
Dryer, R.F.1
Patil, S.R.2
Zellweger, H.U.3
Simpson, J.M.4
Hanson, J.W.5
Aschenbrenner, C.6
Weinstein, S.L.7
-
16
-
-
0019404282
-
Pentasomy X: Report of patient and studies of X-inactivation
-
10.1002/ajmg.1320080105. 7246603
-
Pentasomy X: report of patient and studies of X-inactivation. SJ Funderburk M Valente I Klisak, Am J Med Genet 1981 8 27 33 10.1002/ajmg. 1320080105 7246603
-
(1981)
Am J Med Genet
, vol.8
, pp. 27-33
-
-
Funderburk, S.J.1
Valente, M.2
Klisak, I.3
-
17
-
-
0019952453
-
49,XXXXX syndrome
-
6982661
-
49,XXXXX syndrome. R Fragoso A Hernandez ML Plascencia Z Nazara R Martinez y Martinez JM Cantu, Ann Genet 1982 25 145 148 6982661
-
(1982)
Ann Genet
, vol.25
, pp. 145-148
-
-
Fragoso, R.1
Hernandez, A.2
Plascencia, M.L.3
Nazara, Z.4
Martinez Y Martinez, R.5
Cantu, J.M.6
-
18
-
-
0020263723
-
A case of 49, XXXXX syndrome
-
6819931
-
A case of 49, XXXXX syndrome. RH Zhang NH Pan XF Li XQ Wang M Wu, Chin Med J 1982 95 891 894 6819931
-
(1982)
Chin Med J
, vol.95
, pp. 891-894
-
-
Zhang, R.H.1
Pan, N.H.2
Li, X.F.3
Wang, X.Q.4
Wu, M.5
-
19
-
-
0024686671
-
Penta-X syndrome. Report of a case with 47,XXX/48,XXXX/49,XXXXX mosaicism
-
2665783
-
Penta-X syndrome. Report of a case with 47,XXX/48,XXXX/49,XXXXX mosaicism. L Gomez-Valencia P Najera-Martinez A Morales-Hernandez A Martinez-Diaz De Leon, Bol Med Hosp Infant Mex 1989 46 417 421 2665783
-
(1989)
Bol Med Hosp Infant Mex
, vol.46
, pp. 417-421
-
-
Gomez-Valencia, L.1
Najera-Martinez, P.2
Morales-Hernandez, A.3
Martinez-Diaz De Leon, A.4
-
20
-
-
0025034508
-
Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy
-
10.1007/BF00193591. 1977687
-
Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy. T Hassold D Pettay K May A Robinson, Hum Genet 1990 85 648 650 10.1007/BF00193591 1977687
-
(1990)
Hum Genet
, vol.85
, pp. 648-650
-
-
Hassold, T.1
Pettay, D.2
May, K.3
Robinson, A.4
-
21
-
-
0025760095
-
Parental origin and mechanism of formation of polysomy X: An XXXXX case and four XXXXY cases determined with RFLPs
-
10.1007/BF00201538. 1673956
-
Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs. HX Deng K Abe I Kondo M Tsukahara H Inagaki I Hamada Y Fukushima N Niikawa, Hum Genet 1991 86 541 544 10.1007/BF00201538 1673956
-
(1991)
Hum Genet
, vol.86
, pp. 541-544
-
-
Deng, H.X.1
Abe, K.2
Kondo, I.3
Tsukahara, M.4
Inagaki, H.5
Hamada, I.6
Fukushima, Y.7
Niikawa, N.8
-
22
-
-
0025912632
-
Penta X syndrome: A case report with review of the literature
-
10.1002/ajmg.1320400110. 1887850
-
Penta X syndrome: a case report with review of the literature. R Kassai I Hamada H Furuta K Cho K Abe HX Deng N Niikawa, Am J Med Genet 1991 40 51 56 10.1002/ajmg.1320400110 1887850
-
(1991)
Am J Med Genet
, vol.40
, pp. 51-56
-
-
Kassai, R.1
Hamada, I.2
Furuta, H.3
Cho, K.4
Abe, K.5
Deng, H.X.6
Niikawa, N.7
-
23
-
-
0026924623
-
Pentasomy X mosaic in two adult sisters with diabetes mellitus
-
10.2169/internalmedicine.31.1102. 1421717
-
Pentasomy X mosaic in two adult sisters with diabetes mellitus. S Nakano A Sasame S Azukizawa T Kigoshi K Uchida H Takahashi S Morimoto, Intern Med 1992 31 1102 1106 10.2169/internalmedicine.31.1102 1421717
-
(1992)
Intern Med
, vol.31
, pp. 1102-1106
-
-
Nakano, S.1
Sasame, A.2
Azukizawa, S.3
Kigoshi, T.4
Uchida, K.5
Takahashi, H.6
Morimoto, S.7
-
24
-
-
0027209633
-
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome
-
10.1002/pd.1970130811. 8284294
-
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome. G Martini G Carillo F Catizone A Notarangelo R Mingarelli B Dallapiccola, Prenat Diagn 1993 13 763 766 10.1002/pd.1970130811 8284294
-
(1993)
Prenat Diagn
, vol.13
, pp. 763-766
-
-
Martini, G.1
Carillo, G.2
Catizone, F.3
Notarangelo, A.4
Mingarelli, R.5
Dallapiccola, B.6
-
25
-
-
0029122995
-
Sex chromosome tetrasomy and pentasomy
-
7567329
-
Sex chromosome tetrasomy and pentasomy. MG Linden BG Bender A Robinson, Pediatrics 1995 96 672 682 7567329
-
(1995)
Pediatrics
, vol.96
, pp. 672-682
-
-
Linden, M.G.1
Bender, B.G.2
Robinson, A.3
-
26
-
-
0029116611
-
Dandy-Walker malformation in a fetus with pentasomy X (49,XXXXX) prenatally diagnosed by fluorescence in situ hybridization technique
-
7576173
-
Dandy-Walker malformation in a fetus with pentasomy X (49,XXXXX) prenatally diagnosed by fluorescence in situ hybridization technique. TD Myles L Burd G Font MM McCorquodale DJ McCorquodale, Fetal Diagn Ther 1995 10 333 336 7576173
-
(1995)
Fetal Diagn Ther
, vol.10
, pp. 333-336
-
-
Myles, T.D.1
Burd, L.2
Font, G.3
McCorquodale, M.M.4
McCorquodale, D.J.5
-
27
-
-
0032813598
-
Pentasomy X and hyper IgE syndrome: Co-existence of two distinct genetic disorders
-
10.1007/s004310051187. 10485303
-
Pentasomy X and hyper IgE syndrome: co-existence of two distinct genetic disorders. A Boeck R Gfatter F Braun B Fritz, Eur J Pediatr 1999 158 723 726 10.1007/s004310051187 10485303
-
(1999)
Eur J Pediatr
, vol.158
, pp. 723-726
-
-
Boeck, A.1
Gfatter, R.2
Braun, F.3
Fritz, B.4
-
28
-
-
3843092535
-
Sex chromosome abnormality: Report of three clinical cases of X pentasomy
-
15080523
-
Sex chromosome abnormality: report of three clinical cases of X pentasomy. E Biroli C Ghimenti I Ricci B Pirola ME Liverani A Perona L Galligani A Guala G Angeli, Pathologica 2003 95 444 446 15080523
-
(2003)
Pathologica
, vol.95
, pp. 444-446
-
-
Biroli, E.1
Ghimenti, C.2
Ricci, I.3
Pirola, B.4
Liverani, M.E.5
Perona, A.6
Galligani, L.7
Guala, A.8
Angeli, G.9
-
29
-
-
4444378285
-
A case of 49,XXXXX in which the extra X chromosomes were maternal in origin
-
10.1136/jcp.2004.017475. 15333671
-
A case of 49,XXXXX in which the extra X chromosomes were maternal in origin. YG Cho DS Kim HS Lee SC Cho SI Choi, J Clin Pathol 2004 57 1004 1006 10.1136/jcp.2004.017475 15333671
-
(2004)
J Clin Pathol
, vol.57
, pp. 1004-1006
-
-
Cho, Y.G.1
Kim, D.S.2
Lee, H.S.3
Cho, S.C.4
Choi, S.I.5
-
30
-
-
52349085836
-
X pentasomy in an intracytoplasmic sperm injection pregnancy detected by nuchal translucency testing
-
10.1159/000158653. 18818504
-
X pentasomy in an intracytoplasmic sperm injection pregnancy detected by nuchal translucency testing. PJ Cheng HY Chueh SW Shaw JJ Hsu TT Hsieh YK Soong, Fetal Diagn Ther 2008 24 299 303 10.1159/000158653 18818504
-
(2008)
Fetal Diagn Ther
, vol.24
, pp. 299-303
-
-
Cheng, P.J.1
Chueh, H.Y.2
Shaw, S.W.3
Hsu, J.J.4
Hsieh, T.T.5
Soong, Y.K.6
-
31
-
-
0023746674
-
X-chromosome polysomy in the male. the Leuven experience 1966-1987
-
10.1007/BF00451449. 3417301
-
X-chromosome polysomy in the male. The Leuven experience 1966-1987. A Kleczkowska JP Fryns H Van den Berghe, Hum Genet 1988 80 16 22 10.1007/BF00451449 3417301
-
(1988)
Hum Genet
, vol.80
, pp. 16-22
-
-
Kleczkowska, A.1
Fryns, J.P.2
Den, V.B.H.3
-
32
-
-
7144223296
-
Gene action in the X-chromosome of the mouse (Mus musculus L.)
-
10.1038/190372a0. 13764598
-
Gene action in the X-chromosome of the mouse (Mus musculus L.). MF Lyon, Nature 1961 190 372 373 10.1038/190372a0 13764598
-
(1961)
Nature
, vol.190
, pp. 372-373
-
-
Lyon, M.F.1
-
33
-
-
0016692463
-
Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse
-
10.1038/256640a0. 1152998
-
Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse. N Takagi M Sasaki, Nature 1975 256 640 642 10.1038/256640a0 1152998
-
(1975)
Nature
, vol.256
, pp. 640-642
-
-
Takagi, N.1
Sasaki, M.2
-
35
-
-
0023178599
-
What causes the abnormal phenotype in a 49,XXXXY male?
-
10.1007/BF00283041. 3570296
-
What causes the abnormal phenotype in a 49,XXXXY male? GE Sarto PG Otto EM Kuhn E Therman, Hum Genet 1987 76 1 4 10.1007/BF00283041 3570296
-
(1987)
Hum Genet
, vol.76
, pp. 1-4
-
-
Sarto, G.E.1
Otto, P.G.2
Kuhn, E.M.3
Therman, E.4
-
36
-
-
0018858917
-
X chromosome constitution and the human female phenotype
-
10.1007/BF00278961. 7390488
-
X chromosome constitution and the human female phenotype. E Therman C Denniston GE Sarto M Ulber, Hum Genet 1980 54 133 143 10.1007/BF00278961 7390488
-
(1980)
Hum Genet
, vol.54
, pp. 133-143
-
-
Therman, E.1
Denniston, C.2
Sarto, G.E.3
Ulber, M.4
-
37
-
-
0031689651
-
Histone H4 acetylation analyses in patients with polysomy X: Implications for the mechanism of X inactivation
-
10.1007/s004390050778. 9737772
-
Histone H4 acetylation analyses in patients with polysomy X: implications for the mechanism of X inactivation. CA Leal ML Ayala-Madrigal LE Figuera C Medina, Hum Genet 1998 103 29 33 10.1007/s004390050778 9737772
-
(1998)
Hum Genet
, vol.103
, pp. 29-33
-
-
Leal, C.A.1
Ayala-Madrigal, M.L.2
Figuera, L.E.3
Medina, C.4
-
38
-
-
34249885593
-
Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY
-
10.1002/ajmg.a.31746. 17497714
-
Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY. J Visootsak B Rosner E Dykens N Tartaglia JM Graham Jr, Am J Med Genet 2007 143A 1198 1203 10.1002/ajmg.a.31746 17497714
-
(2007)
Am J Med Genet
, vol.143
, pp. 1198-1203
-
-
Visootsak, J.1
Rosner, B.2
Dykens, E.3
Tartaglia, N.4
-
39
-
-
33644751726
-
Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation
-
10.1038/ncb1365. 16434960
-
Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation. CP Bacher M Guggiari B Brors S Augui P Clerc P Avner R Eils E Heard, Nat Cell Biol 2006 8 293 299 10.1038/ncb1365 16434960
-
(2006)
Nat Cell Biol
, vol.8
, pp. 293-299
-
-
Bacher, C.P.1
Guggiari, M.2
Brors, B.3
Augui, S.4
Clerc, P.5
Avner, P.6
Eils, R.7
Heard, E.8
-
40
-
-
0030723262
-
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation
-
10.1038/ng1197-353. 9354806
-
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation. RM Plenge BD Hendrich C Schwartz JF Arena A Naumova C Sapienza RM Winter HF Willard, Nat Genet 1997 17 353 356 10.1038/ng1197-353 9354806
-
(1997)
Nat Genet
, vol.17
, pp. 353-356
-
-
Plenge, R.M.1
Hendrich, B.D.2
Schwartz, C.3
Arena, J.F.4
Naumova, A.5
Sapienza, C.6
Winter, R.M.7
Willard, H.F.8
-
41
-
-
21044458853
-
Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A
-
10.1038/sj.ejhg.5201386. 15741993
-
Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A. MP Bicocchi BR Migeon M Pasino T Lanza F Bottini E Boeri AC Molinari F Corsolini C Morerio M Acquila, Eur J Hum Genet 2005 13 635 640 10.1038/sj.ejhg.5201386 15741993
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 635-640
-
-
Bicocchi, M.P.1
Migeon, B.R.2
Pasino, M.3
Lanza, T.4
Bottini, F.5
Boeri, E.6
Molinari, A.C.7
Corsolini, F.8
Morerio, C.9
Acquila, M.10
-
42
-
-
0035152359
-
Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients
-
10.1002/1096-8628(20010101)98:1<25::AID-AJMG10153.0.CO;2-X. 11426451
-
Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients. Y Iitsuka A Bock DD Nguyen CA Samango-Sprouse JL Simpson FZ Bischoff, Am J Med Genet 2001 98 25 31 10.1002/1096-8628(20010101)98:1<25: :AID-AJMG10153.0.CO;2-X 11426451
-
(2001)
Am J Med Genet
, vol.98
, pp. 25-31
-
-
Iitsuka, Y.1
Bock, A.2
Nguyen, D.D.3
Samango-Sprouse, C.A.4
Simpson, J.L.5
Bischoff, F.Z.6
-
43
-
-
0016214812
-
Differential condensation of human chromosomes in mitosis under the influence of 5-bromdesoxycytidine
-
4612913
-
Differential condensation of human chromosomes in mitosis under the influence of 5-bromdesoxycytidine. AF Zakharov LI Baranovskaia AI Ibraimov, Tsitologiia 1974 16 1415 1417 4612913
-
(1974)
Tsitologiia
, vol.16
, pp. 1415-1417
-
-
Zakharov, A.F.1
Baranovskaia, L.I.2
Ibraimov, A.I.3
-
44
-
-
0015246254
-
A rapid banding technique for human chromosomes
-
10.1016/S0140-6736(71)90287-X. 4107917
-
A rapid banding technique for human chromosomes. M Seabright, Lancet 1971 2 971 972 10.1016/S0140-6736(71)90287-X 4107917
-
(1971)
Lancet
, vol.2
, pp. 971-972
-
-
Seabright, M.1
-
45
-
-
0016328318
-
New Giemsa method for the differential staining of sister chromatids
-
10.1038/251156a0. 4138930
-
New Giemsa method for the differential staining of sister chromatids. P Perry S Wolff, Nature 1974 251 156 158 10.1038/251156a0 4138930
-
(1974)
Nature
, vol.251
, pp. 156-158
-
-
Perry, P.1
Wolff, S.2
-
46
-
-
0035048037
-
Induction and characterization of hypoxanthine-phosphoribosyltransferase (Hprt-) deficient cell lines of Akodon cursor (Rodentia, Sigmodontinae)
-
10.1159/000056888. 11306816
-
Induction and characterization of hypoxanthine-phosphoribosyltransferase (Hprt-) deficient cell lines of Akodon cursor (Rodentia, Sigmodontinae). CR Bonvicino MA Moreira RA Arcuri HN Seunez, Cytogenet Cell Genet 2001 92 153 156 10.1159/000056888 11306816
-
(2001)
Cytogenet Cell Genet
, vol.92
, pp. 153-156
-
-
Bonvicino, C.R.1
Moreira, M.A.2
Arcuri, R.A.3
Seunez, H.N.4
-
47
-
-
0035885195
-
Molecular analysis of HPRT1(+) somatic cell hybrids derived from a carrier of an HPRT1 mutation responsible for Lesch-Nyhan syndrome
-
10.1002/ajmg.1514. 11562934
-
Molecular analysis of HPRT1(+) somatic cell hybrids derived from a carrier of an HPRT1 mutation responsible for Lesch-Nyhan syndrome. MB Rivero R Olicio CR Lima CR Bonvicino MA Moreira JC Llerena HN Seunez, Am J Med Genet 2001 103 48 55 10.1002/ajmg.1514 11562934
-
(2001)
Am J Med Genet
, vol.103
, pp. 48-55
-
-
Rivero, M.B.1
Olicio, R.2
Lima, C.R.3
Bonvicino, C.R.4
Moreira, M.A.5
Llerena, J.C.6
Seunez, H.N.7
-
49
-
-
0024205612
-
The human androgen receptor: Complementary deoxyribonucleic acid cloning, sequence analysis and gene expression in prostate
-
10.1210/mend-2-12-1265. 3216866
-
The human androgen receptor: complementary deoxyribonucleic acid cloning, sequence analysis and gene expression in prostate. DB Lubahn, Mol Endocrinol 1988 2 1265 1275 10.1210/mend-2-12-1265 3216866
-
(1988)
Mol Endocrinol
, vol.2
, pp. 1265-1275
-
-
Lubahn, D.B.1
-
50
-
-
0029088029
-
Quantitative non-radioactive clonality analysis of human leukemic cells and progenitors using the human androgen receptor (AR) gene
-
7658727
-
Quantitative non-radioactive clonality analysis of human leukemic cells and progenitors using the human androgen receptor (AR) gene. E Delabesse S Aral P Kamoun B Varet AG Turhan, Leukemia 1995 9 1578 1582 7658727
-
(1995)
Leukemia
, vol.9
, pp. 1578-1582
-
-
Delabesse, E.1
Aral, S.2
Kamoun, P.3
Varet, B.4
Turhan, A.G.5
-
52
-
-
34547781750
-
MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0
-
10.1093/molbev/msm092. 17488738
-
MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. K Tamura J Dudley M Nei S Kumar, Mol Biol Evol 2007 24 1596 1599 10.1093/molbev/msm092 17488738
-
(2007)
Mol Biol Evol
, vol.24
, pp. 1596-1599
-
-
Tamura, K.1
Dudley, J.2
Nei, M.3
Kumar, S.4
|