-
1
-
-
0025364886
-
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif
-
Sinclair A.H., Berta P., Palmer M.S., Hawkins J.R., Griffiths B.L., Smith M.J., et al. A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif. Nature 346 (1990) 240-244
-
(1990)
Nature
, vol.346
, pp. 240-244
-
-
Sinclair, A.H.1
Berta, P.2
Palmer, M.S.3
Hawkins, J.R.4
Griffiths, B.L.5
Smith, M.J.6
-
3
-
-
0019422956
-
The etiology of maleness in XX men
-
de la Chapelle A. The etiology of maleness in XX men. Hum Genet 58 (1981) 105-106
-
(1981)
Hum Genet
, vol.58
, pp. 105-106
-
-
de la Chapelle, A.1
-
4
-
-
0025097016
-
A possible common origin of "Y-negative" human XX males and XX true hermaphrodites
-
Abbas N.E., Toublanc J.E., Boucekkine C., Toublanc M., Affara N.A., Job J.C., et al. A possible common origin of "Y-negative" human XX males and XX true hermaphrodites. Hum Genet 84 (1990) 356-360
-
(1990)
Hum Genet
, vol.84
, pp. 356-360
-
-
Abbas, N.E.1
Toublanc, J.E.2
Boucekkine, C.3
Toublanc, M.4
Affara, N.A.5
Job, J.C.6
-
5
-
-
0028304515
-
Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences
-
Boucekkine C., Toublanc J.E., Abbas N., Chaabouni S., Ouahid S., Semrouni M., et al. Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences. Clin Endocrinol (Oxf) 40 (1994) 733-742
-
(1994)
Clin Endocrinol (Oxf)
, vol.40
, pp. 733-742
-
-
Boucekkine, C.1
Toublanc, J.E.2
Abbas, N.3
Chaabouni, S.4
Ouahid, S.5
Semrouni, M.6
-
6
-
-
0026793969
-
A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY
-
McElreavey K., Rappaport R., Vilain E., Abbas N., Richaud F., Lortat-Jacob S., et al. A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY. Hum Genet 90 (1992) 121-125
-
(1992)
Hum Genet
, vol.90
, pp. 121-125
-
-
McElreavey, K.1
Rappaport, R.2
Vilain, E.3
Abbas, N.4
Richaud, F.5
Lortat-Jacob, S.6
-
7
-
-
0027466437
-
A regulatory cascade hypothesis for mammalian sex determination. SRY represses a negative regulator of male development
-
McElreavey K., Vilain E., Abbas N., Herskowitz I., and Fellous M. A regulatory cascade hypothesis for mammalian sex determination. SRY represses a negative regulator of male development. Proc Natl Acad Sci USA 90 (1993) 3368-3372
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 3368-3372
-
-
McElreavey, K.1
Vilain, E.2
Abbas, N.3
Herskowitz, I.4
Fellous, M.5
-
8
-
-
2642680023
-
Two SRY-negative XX male brothers without genital ambiguity
-
Zenteno J.C., Lopez M., Vera C., Mendez J.P., and Kofman-Alfaro S. Two SRY-negative XX male brothers without genital ambiguity. Hum Genet 100 (1997) 606-610
-
(1997)
Hum Genet
, vol.100
, pp. 606-610
-
-
Zenteno, J.C.1
Lopez, M.2
Vera, C.3
Mendez, J.P.4
Kofman-Alfaro, S.5
-
9
-
-
0032323373
-
Clinical and molecular analysis of XX sex reversed patients
-
discussion 1178
-
Kolon T.F., Ferrer F.A., and McKenna P.H. Clinical and molecular analysis of XX sex reversed patients. J Urol 160 (1998) 1169-1172 discussion 1178
-
(1998)
J Urol
, vol.160
, pp. 1169-1172
-
-
Kolon, T.F.1
Ferrer, F.A.2
McKenna, P.H.3
-
10
-
-
0033981864
-
An SRY-negative XX male with Huriez syndrome
-
Vernole P., Terrinoni A., Didona B., De Laurenzi V., Rossi P., Melino G., et al. An SRY-negative XX male with Huriez syndrome. Clin Genet 57 (2000) 61-66
-
(2000)
Clin Genet
, vol.57
, pp. 61-66
-
-
Vernole, P.1
Terrinoni, A.2
Didona, B.3
De Laurenzi, V.4
Rossi, P.5
Melino, G.6
-
11
-
-
0035075031
-
XX males without SRY gene and with infertility
-
Abusheikha N., Lass A., and Brinsden P. XX males without SRY gene and with infertility. Hum Reprod 16 (2001) 717-718
-
(2001)
Hum Reprod
, vol.16
, pp. 717-718
-
-
Abusheikha, N.1
Lass, A.2
Brinsden, P.3
-
12
-
-
0242522155
-
Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI. case report
-
Ma S., Tang S.S., Yuen B.H., Bruyere H., Penaherrera M., and Robinson W.P. Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI. case report. Hum Reprod 18 (2003) 2298-2301
-
(2003)
Hum Reprod
, vol.18
, pp. 2298-2301
-
-
Ma, S.1
Tang, S.S.2
Yuen, B.H.3
Bruyere, H.4
Penaherrera, M.5
Robinson, W.P.6
-
13
-
-
11844303535
-
A 46,XX SRY-negative man with complete virilization and infertility as the main anomaly
-
Valetto A., Bertini V., Rapalini E., and Simi P. A 46,XX SRY-negative man with complete virilization and infertility as the main anomaly. Fertil Steril 83 (2005) 216-219
-
(2005)
Fertil Steril
, vol.83
, pp. 216-219
-
-
Valetto, A.1
Bertini, V.2
Rapalini, E.3
Simi, P.4
-
14
-
-
0026545968
-
Extensive cross-homology between the long and the short arm of chromosome 16 may explain leukemic inversions and translocations
-
Dauwerse J.G., Jumelet E.A., Wessels J.W., Saris J.J., Hagemeijer A., Beverstock G.C., et al. Extensive cross-homology between the long and the short arm of chromosome 16 may explain leukemic inversions and translocations. Blood 79 (1992) 1299-1304
-
(1992)
Blood
, vol.79
, pp. 1299-1304
-
-
Dauwerse, J.G.1
Jumelet, E.A.2
Wessels, J.W.3
Saris, J.J.4
Hagemeijer, A.5
Beverstock, G.C.6
-
15
-
-
0014029835
-
X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome
-
Ferguson-Smith M.A. X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome. Lancet 2 (1966) 475-476
-
(1966)
Lancet
, vol.2
, pp. 475-476
-
-
Ferguson-Smith, M.A.1
-
17
-
-
0033988508
-
SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite
-
Margarit E., Coll M.D., Oliva R., Gomez D., Soler A., and Ballesta F. SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite. Am J Med Genet 90 (2000) 25-28
-
(2000)
Am J Med Genet
, vol.90
, pp. 25-28
-
-
Margarit, E.1
Coll, M.D.2
Oliva, R.3
Gomez, D.4
Soler, A.5
Ballesta, F.6
-
18
-
-
12944333125
-
Alpha-thalassemia/mental retardation syndrome in a 45,X male
-
Kellermayer R., Czako M., Kiss-Laszlo Z., Gyuris P., Kozari A., Melegh B., et al. Alpha-thalassemia/mental retardation syndrome in a 45,X male. Am J Med Genet A 132 (2005) 431-433
-
(2005)
Am J Med Genet A
, vol.132
, pp. 431-433
-
-
Kellermayer, R.1
Czako, M.2
Kiss-Laszlo, Z.3
Gyuris, P.4
Kozari, A.5
Melegh, B.6
-
19
-
-
0027375457
-
A 45,X male with an X;Y translocation. implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata
-
Weil D., Portnoi M.F., Levilliers J., Wang I., Mathieu M., Taillemite J.L., et al. A 45,X male with an X;Y translocation. implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata. Hum Mol Genet 2 (1993) 1853-1856
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1853-1856
-
-
Weil, D.1
Portnoi, M.F.2
Levilliers, J.3
Wang, I.4
Mathieu, M.5
Taillemite, J.L.6
-
20
-
-
0032833672
-
The plasticity of human telomeres demonstrated by a hypervariable telomere repeat array that is located on some copies of 16p and 16q
-
Coleman J., Baird D.M., and Royle N.J. The plasticity of human telomeres demonstrated by a hypervariable telomere repeat array that is located on some copies of 16p and 16q. Hum Mol Genet 8 (1999) 1637-1646
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1637-1646
-
-
Coleman, J.1
Baird, D.M.2
Royle, N.J.3
|