-
2
-
-
0028876968
-
New genes for boys
-
Sinclair A.H. New genes for boys. Am J Hum Genet. 57:1995;998-1001.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 998-1001
-
-
Sinclair, A.H.1
-
3
-
-
0029083703
-
In situ hybridization analysis of the Y chromosome in gonadoblastoma
-
Sultana R., Myerson D., Disteche C.M. In situ hybridization analysis of the Y chromosome in gonadoblastoma. Genes Chromosomes Cancer. 13:1995;257-262.
-
(1995)
Genes Chromosomes Cancer
, vol.13
, pp. 257-262
-
-
Sultana, R.1
Myerson, D.2
Disteche, C.M.3
-
4
-
-
0030833849
-
Gonadoblastomas in 45,X/46,XY mosaicism: Analysis of Y chromosome distribution by fluorescence in situ hybridization
-
Iezzoni J.C., Von Kap-Herr C., Golden W.L., Gaffey M.J. Gonadoblastomas in 45,X/46,XY mosaicism. analysis of Y chromosome distribution by fluorescence in situ hybridization Am J Clin Pathol. 108:1997;197-201.
-
(1997)
Am J Clin Pathol
, vol.108
, pp. 197-201
-
-
Iezzoni, J.C.1
Von Kap-Herr, C.2
Golden, W.L.3
Gaffey, M.J.4
-
6
-
-
0034049679
-
The molecular basis of male sexual differentiation
-
Hiort O., Holterhaus P.M. The molecular basis of male sexual differentiation. Eur J Endocrinol. 142:2000;101-110.
-
(2000)
Eur J Endocrinol
, vol.142
, pp. 101-110
-
-
Hiort, O.1
Holterhaus, P.M.2
-
7
-
-
0028864744
-
3-Year-old phenotypic female with campomelic dysplasia and bilateral gonadoblastoma
-
Hong J.R., Barber M., Scott C.I., Guttenberg M., Wolfson P.J. 3-Year-old phenotypic female with campomelic dysplasia and bilateral gonadoblastoma. J Pediatr Surg. 30:1995;1735-1737.
-
(1995)
J Pediatr Surg
, vol.30
, pp. 1735-1737
-
-
Hong, J.R.1
Barber, M.2
Scott, C.I.3
Guttenberg, M.4
Wolfson, P.J.5
-
8
-
-
0014119131
-
Association d'un syndrome anatomo-pathologique de pseudohermaphrodisme masculin, d'une tumeur de Wilms, d'une nephropathie parenchymateuse et d'un mosaicisme XX/XY
-
Denys P., Malvaux P., van den Berghe H., Tanghe W., Proesmans W. Association d'un syndrome anatomo-pathologique de pseudohermaphrodisme masculin, d'une tumeur de Wilms, d'une nephropathie parenchymateuse et d'un mosaicisme XX/XY. Arch Fr Pediatr. 24:1967;729-739.
-
(1967)
Arch Fr Pediatr
, vol.24
, pp. 729-739
-
-
Denys, P.1
Malvaux, P.2
Van den Berghe, H.3
Tanghe, W.4
Proesmans, W.5
-
9
-
-
0014775569
-
A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease
-
Drash A., Sherman F., Hartmann W.H., Blizzard R.M. A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease. J Pediatr. 76:1970;585-593.
-
(1970)
J Pediatr
, vol.76
, pp. 585-593
-
-
Drash, A.1
Sherman, F.2
Hartmann, W.H.3
Blizzard, R.M.4
-
10
-
-
0000786264
-
Gonadoblastoma associated with pure gonadal dysgenesis in monozygotic twins
-
Frasier S.D., Bashore R.A., Mosier H.D. Gonadoblastoma associated with pure gonadal dysgenesis in monozygotic twins. J Pediatr. 64:1964;740-745.
-
(1964)
J Pediatr
, vol.64
, pp. 740-745
-
-
Frasier, S.D.1
Bashore, R.A.2
Mosier, H.D.3
-
11
-
-
0027198809
-
Complete and partial 46,XY sex reversal associated with terminal deletion of 10q: Report of 2 cases and literature review
-
Wilkie A.O., Campbell F.M., Daubeney P., Grant D.B., Daniels R.J., Mullarkey M., Afara N.A., Fitchett M., Huson S.M. Complete and partial 46,XY sex reversal associated with terminal deletion of 10q. report of 2 cases and literature review Am J Med Genet. 15:1993;597-600.
-
(1993)
Am J Med Genet
, vol.15
, pp. 597-600
-
-
Wilkie, A.O.1
Campbell, F.M.2
Daubeney, P.3
Grant, D.B.4
Daniels, R.J.5
Mullarkey, M.6
Afara, N.A.7
Fitchett, M.8
Huson, S.M.9
-
12
-
-
0031962673
-
Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: Report of a case
-
Chung Y.P., Hwa H.L., Tseng L.H., Shyu M.K., Lee C.N., Shih J.C., Hsieh F.J. Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal. report of a case Prenat Diagn. 18:1998;73-77.
-
(1998)
Prenat Diagn
, vol.18
, pp. 73-77
-
-
Chung, Y.P.1
Hwa, H.L.2
Tseng, L.H.3
Shyu, M.K.4
Lee, C.N.5
Shih, J.C.6
Hsieh, F.J.7
-
13
-
-
0023734622
-
Eleven new cases of del(9p) and features from 80 cases
-
Huret J.L., Leonard C., Forestier B., Rethore M.O., Lejeune J. Eleven new cases of del(9p) and features from 80 cases. J Med Genet. 25:1988;741-749.
-
(1988)
J Med Genet
, vol.25
, pp. 741-749
-
-
Huret, J.L.1
Leonard, C.2
Forestier, B.3
Rethore, M.O.4
Lejeune, J.5
-
14
-
-
0030703261
-
XY sex reversal monosomy and gonadal dysgenesis due to 9p24 monosomy
-
McDonald T.M., Flejter W., Sheldon S., Putzi J.P., Gorski L.J. XY sex reversal monosomy and gonadal dysgenesis due to 9p24 monosomy. Am J Med Genet. 73:1997;321-326.
-
(1997)
Am J Med Genet
, vol.73
, pp. 321-326
-
-
McDonald, T.M.1
Flejter, W.2
Sheldon, S.3
Putzi, J.P.4
Gorski, L.J.5
-
15
-
-
0033678603
-
Sex-determining gene(s) on distal 9p: Clinical and molecular studies in six cases
-
Muroya K., Okuyama T., Goishi K., Ogiso Y., Fukuda S., Kameyama J., Sato H., Suzuki Y., Terasaki H., Gomyo H., Wakui K., Fukushima Y., Ogata T. Sex-determining gene(s) on distal 9p. clinical and molecular studies in six cases J Clin Endocrinol Metab. 85:2000;3094-3100.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 3094-3100
-
-
Muroya, K.1
Okuyama, T.2
Goishi, K.3
Ogiso, Y.4
Fukuda, S.5
Kameyama, J.6
Sato, H.7
Suzuki, Y.8
Terasaki, H.9
Gomyo, H.10
Wakui, K.11
Fukushima, Y.12
Ogata, T.13
-
17
-
-
0032509983
-
Evidence for evolutionary conservation of sex-determining genes
-
Raymond C.S., Shamu C.E., Shen M.M., Seifert K.J., Hirsch B., Hodgkin J., Zarkower D. Evidence for evolutionary conservation of sex-determining genes. Nature. 391:1998;691-695.
-
(1998)
Nature
, vol.391
, pp. 691-695
-
-
Raymond, C.S.1
Shamu, C.E.2
Shen, M.M.3
Seifert, K.J.4
Hirsch, B.5
Hodgkin, J.6
Zarkower, D.7
-
18
-
-
0034193607
-
A new submicroscopic deletion that refines the 9p region for sex reversal
-
Calvari V., Bertini V., De Grandi A., Peverali G., Zuffardi O., Ferguson-Smith M., Knudtzon J., Camerino G., Borsani G., Guioli S. A new submicroscopic deletion that refines the 9p region for sex reversal. Genomics. 5:2000;203-212.
-
(2000)
Genomics
, vol.5
, pp. 203-212
-
-
Calvari, V.1
Bertini, V.2
De Grandi, A.3
Peverali, G.4
Zuffardi, O.5
Ferguson-Smith, M.6
Knudtzon, J.7
Camerino, G.8
Borsani, G.9
Guioli, S.10
-
19
-
-
0034077305
-
FISH mapping of the sex-reversal region on human chromosome 9 in two XY females and in primates
-
Shan Z., Zabel B., Trautmann U., Hillig U., Ottolenghi C., Wan Y., Haaf T. FISH mapping of the sex-reversal region on human chromosome 9 in two XY females and in primates. Eur J Hum Genet. 3:2000;167-173.
-
(2000)
Eur J Hum Genet
, vol.3
, pp. 167-173
-
-
Shan, Z.1
Zabel, B.2
Trautmann, U.3
Hillig, U.4
Ottolenghi, C.5
Wan, Y.6
Haaf, T.7
-
20
-
-
0033357990
-
Chromosome breakage hotspots and delineation of the critical region for the 9p- deletion syndrome
-
Christ L.A., Crowe C.A., Micale M.A., Conroy J.M., Schwartz S. Chromosome breakage hotspots and delineation of the critical region for the 9p- deletion syndrome. Am J Hum Genet. 65:1999;1387-1395.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1387-1395
-
-
Christ, L.A.1
Crowe, C.A.2
Micale, M.A.3
Conroy, J.M.4
Schwartz, S.5
-
21
-
-
0033009983
-
A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators
-
Raymond C.S., Parker E.D., Kettlewell J.R., Brown L.G., Page D.C., Kusz K., Jaruzelska J., Reinberg Y., Flejter W.L., Bardwell V.J., Hirsch B., Zarkower D. A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators. Hum Mol Genet. 8:1999;989-996.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 989-996
-
-
Raymond, C.S.1
Parker, E.D.2
Kettlewell, J.R.3
Brown, L.G.4
Page, D.C.5
Kusz, K.6
Jaruzelska, J.7
Reinberg, Y.8
Flejter, W.L.9
Bardwell, V.J.10
Hirsch, B.11
Zarkower, D.12
-
22
-
-
0022467814
-
Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversal
-
Fryns J.P., Kleczkowska A., Caesar P., v d Berghe H. Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversal. Ann Genet. 29:1986;49-52.
-
(1986)
Ann Genet
, vol.29
, pp. 49-52
-
-
Fryns, J.P.1
Kleczkowska, A.2
Caesar, P.3
Berghe, V.D.H.4
-
23
-
-
0027316087
-
Deletion 9p and sex reversal
-
Bennett C.P., Docherty Z., Robb S.A., Ramani P., Hawkins J.R., Grant D. Deletion 9p and sex reversal. J Med Genet. 30:1993;518-520.
-
(1993)
J Med Genet
, vol.30
, pp. 518-520
-
-
Bennett, C.P.1
Docherty, Z.2
Robb, S.A.3
Ramani, P.4
Hawkins, J.R.5
Grant, D.6
-
24
-
-
0030957133
-
Impaired male sex development in an infant with molecularly defined partial 9p monosomy: Implications for a testis forming gene(s) on 9p
-
Ogata T., Muroya K., Matsuo N., Hata J., Fukushima Y., Suzuki Y. Impaired male sex development in an infant with molecularly defined partial 9p monosomy. implications for a testis forming gene(s) on 9p J Med Genet. 34:1997;331-334.
-
(1997)
J Med Genet
, vol.34
, pp. 331-334
-
-
Ogata, T.1
Muroya, K.2
Matsuo, N.3
Hata, J.4
Fukushima, Y.5
Suzuki, Y.6
-
25
-
-
0031947449
-
Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene
-
Ion R., Telvi L., Chaussain J.L., Barbet J.P., Nunes M., Safar A., Rethore M.O., Fellous M., McElreavey K. Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene. Hum Genet. 102:1998;151-156.
-
(1998)
Hum Genet
, vol.102
, pp. 151-156
-
-
Ion, R.1
Telvi, L.2
Chaussain, J.L.3
Barbet, J.P.4
Nunes, M.5
Safar, A.6
Rethore, M.O.7
Fellous, M.8
McElreavey, K.9
-
26
-
-
0033003575
-
Defective sexual development in an infant with 46,XY,der(9)t(8;9)(q23.1;p23)mat
-
Pfeiffer R.A., Rauch A., Trautmann U., Dorr H.G., Hiort O., Scherer G., Rosch G., Papadopoulos T., v d Hardt K., Lachmann E. Defective sexual development in an infant with 46,XY,der(9)t(8;9)(q23.1;p23)mat. Eur J Pediatr. 158:1999;213-216.
-
(1999)
Eur J Pediatr
, vol.158
, pp. 213-216
-
-
Pfeiffer, R.A.1
Rauch, A.2
Trautmann, U.3
Dorr, H.G.4
Hiort, O.5
Scherer, G.6
Rosch, G.7
Papadopoulos, T.8
Hardt, V.D.K.9
Lachmann, E.10
-
27
-
-
0031569887
-
Deletions of distal 9p associated with 46,XY male to female sex reversal: Definition of the breakpoints at 9p23.3-p24.1
-
Veitia R., Nunes M., Brauner R., Doco-Fenzy M., Joanny-Fillinois O., Laubert F., Lortat-Jacob S., Fellous M., McElreavy K. Deletions of distal 9p associated with 46,XY male to female sex reversal. definition of the breakpoints at 9p23.3-p24.1 Genomics. 41:1997;271-274.
-
(1997)
Genomics
, vol.41
, pp. 271-274
-
-
Veitia, R.1
Nunes, M.2
Brauner, R.3
Doco-Fenzy, M.4
Joanny-Fillinois, O.5
Laubert, F.6
Lortat-Jacob, S.7
Fellous, M.8
McElreavy, K.9
-
28
-
-
0017681544
-
46,XY,r(9) in a male with ambiguous external genitalia
-
Metaxotou C., Kalpini-Mavrou A. 46,XY,r(9) in a male with ambiguous external genitalia. Hum Genet. 37:1977;351-354.
-
(1977)
Hum Genet
, vol.37
, pp. 351-354
-
-
Metaxotou, C.1
Kalpini-Mavrou, A.2
-
29
-
-
0023807124
-
An unbalanced autosomal translocation (7;9) associated with feminization
-
Crocker M., Coghill S.B., Cortinho R. An unbalanced autosomal translocation (7;9) associated with feminization. Clin Genet. 34:1988;70-73.
-
(1988)
Clin Genet
, vol.34
, pp. 70-73
-
-
Crocker, M.1
Coghill, S.B.2
Cortinho, R.3
-
30
-
-
0033921841
-
Ovarian gonadoblastoma with mixed germ cell tumor in a woman with 46,XX karyotype and successful pregnancies
-
Zhao S., Kato N., Endoh Y., Jin Z., Ajioka Y., Motoyama T. Ovarian gonadoblastoma with mixed germ cell tumor in a woman with 46,XX karyotype and successful pregnancies. Pathol Int. 50:2000;332-335.
-
(2000)
Pathol Int
, vol.50
, pp. 332-335
-
-
Zhao, S.1
Kato, N.2
Endoh, Y.3
Jin, Z.4
Ajioka, Y.5
Motoyama, T.6
-
31
-
-
0033709679
-
Occurrence of gonadoblastoma in females with Turner syndrome and Y chromosome material: A population study
-
Gravholt C.H., Fedder J., Naeraa R.W., Muller J. Occurrence of gonadoblastoma in females with Turner syndrome and Y chromosome material. a population study J Clin Endocrinol Metab. 85:2000;3199-3202.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 3199-3202
-
-
Gravholt, C.H.1
Fedder, J.2
Naeraa, R.W.3
Muller, J.4
-
32
-
-
0028807452
-
Gonadoblastoma: Molecular definition of the susceptibility region on the Y chromosome
-
Tsuchiya K., Reijo R., Page D.C., Disteche C.M. Gonadoblastoma. molecular definition of the susceptibility region on the Y chromosome Am J Hum Genet. 57:1995;1400-1407.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1400-1407
-
-
Tsuchiya, K.1
Reijo, R.2
Page, D.C.3
Disteche, C.M.4
-
33
-
-
0034488388
-
Expression of a candidate gene for the gonadoblastoma locus in gonadoblastoma and testicular seminoma
-
Lau Y., Chou P., Iezzoni J., Alonzo J., Komuves L. Expression of a candidate gene for the gonadoblastoma locus in gonadoblastoma and testicular seminoma. Cytogenet Cell Genet. 91:2000;160-164.
-
(2000)
Cytogenet Cell Genet
, vol.91
, pp. 160-164
-
-
Lau, Y.1
Chou, P.2
Iezzoni, J.3
Alonzo, J.4
Komuves, L.5
-
34
-
-
0345149000
-
Detection of TSPY protein in a unilateral microscopic gonadoblastoma of a Turner mosaic patient with a Y-derived marker chromosome
-
Hildenbrand R., Schroder W., Brude E., Schepler A., Konig R., Stutte H.J. Detection of TSPY protein in a unilateral microscopic gonadoblastoma of a Turner mosaic patient with a Y-derived marker chromosome. J Pathol. 189:1999;623-626.
-
(1999)
J Pathol
, vol.189
, pp. 623-626
-
-
Hildenbrand, R.1
Schroder, W.2
Brude, E.3
Schepler, A.4
Konig, R.5
Stutte, H.J.6
-
35
-
-
0033365196
-
Gonadoblastoma, testicular and prostate cancers and the TSPY gene
-
Lau Y. Gonadoblastoma, testicular and prostate cancers and the TSPY gene. Am J Hum Genet. 64:1999;921-927.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 921-927
-
-
Lau, Y.1
-
36
-
-
0030020856
-
High frequency of chromosome 9 deletion in ovarian cancer: Evidence for three tumour-suppressor loci
-
Devlin J., Elder P.A., Gabra H., Steel C.M., Knowles M.A. High frequency of chromosome 9 deletion in ovarian cancer. evidence for three tumour-suppressor loci Br J Cancer. 73:1996;420-423.
-
(1996)
Br J Cancer
, vol.73
, pp. 420-423
-
-
Devlin, J.1
Elder, P.A.2
Gabra, H.3
Steel, C.M.4
Knowles, M.A.5
-
37
-
-
13044266372
-
Association of chromosome arm 9p abnormalities with adverse risk in childhood acute lymphoblastic leukemia: A report from the Children's Cancer Group
-
Heerema N.A., Sather H.N., Sensel M.G., Liu-Mares W., Lange B.J., Bostrom B.C., Nachman J.B., Steiherz P.G., Hutchinson R., Gaynon P.S., Arthur D.C., Uckun F.M. Association of chromosome arm 9p abnormalities with adverse risk in childhood acute lymphoblastic leukemia. a report from the Children's Cancer Group Blood. 94:1999;1537-1544.
-
(1999)
Blood
, vol.94
, pp. 1537-1544
-
-
Heerema, N.A.1
Sather, H.N.2
Sensel, M.G.3
Liu-Mares, W.4
Lange, B.J.5
Bostrom, B.C.6
Nachman, J.B.7
Steiherz, P.G.8
Hutchinson, R.9
Gaynon, P.S.10
Arthur, D.C.11
Uckun, F.M.12
-
38
-
-
0032959540
-
Risk of gonadoblastoma in female patients with Y chromosome abnormalities and dysgenetic gonads
-
Gibbons B., Tan S.Y., Yu C.C., Cheah E., Tan H.L. Risk of gonadoblastoma in female patients with Y chromosome abnormalities and dysgenetic gonads. J Paediatr Child Health. 35:1999;210-213.
-
(1999)
J Paediatr Child Health
, vol.35
, pp. 210-213
-
-
Gibbons, B.1
Tan, S.Y.2
Yu, C.C.3
Cheah, E.4
Tan, H.L.5
-
39
-
-
0342980244
-
Management of males with 45,X/46,XY gonadal dysgenesis
-
Muller J., Ritzen E.M., Ivarsson S.A., Rajpert-De Meyts E., Norjavaara E., Skakkebaek N.E. Management of males with 45,X/46,XY gonadal dysgenesis. Horm Res. 52:1999;11-14.
-
(1999)
Horm Res
, vol.52
, pp. 11-14
-
-
Muller, J.1
Ritzen, E.M.2
Ivarsson, S.A.3
Rajpert-De Meyts, E.4
Norjavaara, E.5
Skakkebaek, N.E.6
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