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Aktas, D., Alikasifoglu, M., Gonc, N. és mtsai: Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis. Eur. J. Med. Genet., 2006, 49, 141-149.
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Aktas, D., Alikasifoglu, M., Gonc, N. és mtsai: Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis. Eur. J. Med. Genet., 2006, 49, 141-149.
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2
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Alvarez-Nava, F., Soto, M., Martinez, M. C. és mtsai: FISH and PCR analyses in three patients with 45, X/46, X, idic(Y) karyotype: clinical and pathologic spectrum. Ann. Genet., 2003, 46, 443-448.
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Alvarez-Nava, F., Soto, M., Martinez, M. C. és mtsai: FISH and PCR analyses in three patients with 45, X/46, X, idic(Y) karyotype: clinical and pathologic spectrum. Ann. Genet., 2003, 46, 443-448.
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3
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Different chromosome Y abnormalities in Turner syndrome
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Bagei, G., Acar, H., Tomruk, H.: Different chromosome Y abnormalities in Turner syndrome. Genet. Couns., 2001, 12, 255-261.
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Canto, P., Galicia, N., Soderlund, D. és mtsai: Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicism. Eur. J. Obstet. Gynecol. Reprod. Biol., 2004, 115, 55-58.
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Canto, P., Galicia, N., Soderlund, D. és mtsai: Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicism. Eur. J. Obstet. Gynecol. Reprod. Biol., 2004, 115, 55-58.
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Canto, P., Vilchis, F., Soderlund, D. és mtsai: A heterozygous mutation in the desert hedgehog gene in patients with mixed gonadal dysgenesis. Mol. Hum. Reprod., 2005, 11, 833-836.
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Canto, P., Vilchis, F., Soderlund, D. és mtsai: A heterozygous mutation in the desert hedgehog gene in patients with mixed gonadal dysgenesis. Mol. Hum. Reprod., 2005, 11, 833-836.
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6
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Dundar, M., Lowther, G., Acar, H. és mtsai: A case of ambiguous genitalia presenting with a 45, X/46, Xr(Y)(p11.2; q11.23)/ 47, X, idic(Y) (p11.2), idic(Y)(p11.2) karyotype. Ann. Genet., 2001, 44, 5-8.
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Dundar, M., Lowther, G., Acar, H. és mtsai: A case of ambiguous genitalia presenting with a 45, X/46, Xr(Y)(p11.2; q11.23)/ 47, X, idic(Y) (p11.2), idic(Y)(p11.2) karyotype. Ann. Genet., 2001, 44, 5-8.
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7
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Hernando, C., Carrera, M., Ribas, I. és mtsai: Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis. Prenat. Diagn., 2002, 22, 802-805.
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Hernando, C., Carrera, M., Ribas, I. és mtsai: Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis. Prenat. Diagn., 2002, 22, 802-805.
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8
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Kirsch, S., Weiss, B., De Rosa, M. és mtsai: FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY. J. Med. Genet., 2000, 37, 593-599.
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Kirsch, S., Weiss, B., De Rosa, M. és mtsai: FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY. J. Med. Genet., 2000, 37, 593-599.
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9
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Kolon, T. F., Gray, C. L., Borboroglu, P. G.: Prenatal karyotype and ultrasound discordance in intersex conditions. Urology, 1999, 54, 1097xvi-1097xix.
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Kolon, T. F., Gray, C. L., Borboroglu, P. G.: Prenatal karyotype and ultrasound discordance in intersex conditions. Urology, 1999, 54, 1097xvi-1097xix.
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10
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Marcus-Soekarman, D., Hamers, G., Mulder, A. L. és mtsai: Sonographic genital ambiguity in a fetus due to a mosaic 45, X/46, X, idic(Y)(qter-p11.32: p11.32-qter) karyotype. Prenat. Diagn., 2005, 25, 279-282.
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Marcus-Soekarman, D., Hamers, G., Mulder, A. L. és mtsai: Sonographic genital ambiguity in a fetus due to a mosaic 45, X/46, X, idic(Y)(qter-p11.32: p11.32-qter) karyotype. Prenat. Diagn., 2005, 25, 279-282.
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11
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Marrocco, G., Poscente, M., Majore, S. és mtsai: Clinical management and molecular cytogenetic characterization in a 45, X/46, X, idic(Yp) patient with severe hypospadia. J. Pediatr. Surg., 2003, 38, 1258-1262.
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Marrocco, G., Poscente, M., Majore, S. és mtsai: Clinical management and molecular cytogenetic characterization in a 45, X/46, X, idic(Yp) patient with severe hypospadia. J. Pediatr. Surg., 2003, 38, 1258-1262.
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12
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Raff, R., Schubert, R., Schwanitz, G. és mtsai: Combination of hypospadias and maldescended testis as cardinal symptoms in gonosomal chromosome aberrations. Eur. J. Pediatr. Surg., 2000, 70, 270-275.
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Raff, R., Schubert, R., Schwanitz, G. és mtsai: Combination of hypospadias and maldescended testis as cardinal symptoms in gonosomal chromosome aberrations. Eur. J. Pediatr. Surg., 2000, 70, 270-275.
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13
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Rivera, H., Ayala-Madrigal, L. M., Gutierrez-Angulo, M. és mtsai: Isodicentric Y chromosomes and secondary microchromosomes. Genet. Couns., 2003, 14, 227-231.
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Rivera, H., Ayala-Madrigal, L. M., Gutierrez-Angulo, M. és mtsai: Isodicentric Y chromosomes and secondary microchromosomes. Genet. Couns., 2003, 14, 227-231.
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14
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0342502138
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Stankiewicz, P., Helias-Rodzewicz, Z., Jakubow-Durska, K. és mtsai: Cytogenetic and molecular characterization of two isodicentric Y chromosomes. Am. J. Med. Genet., 2001, 101, 20-25.
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Stankiewicz, P., Helias-Rodzewicz, Z., Jakubow-Durska, K. és mtsai: Cytogenetic and molecular characterization of two isodicentric Y chromosomes. Am. J. Med. Genet., 2001, 101, 20-25.
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15
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Queipo, G., Nieto, K., Grether, P. és mtsai: Unusual mixed gonadal dysgenesis associated with Mullerian duct persistence, polygonadia, and a 45, X/46, X, idic(Y)(p) karyotype. Am. J. Med. Genet., 2005, 136, 386-389.
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Queipo, G., Nieto, K., Grether, P. és mtsai: Unusual mixed gonadal dysgenesis associated with Mullerian duct persistence, polygonadia, and a 45, X/46, X, idic(Y)(p) karyotype. Am. J. Med. Genet., 2005, 136, 386-389.
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16
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Tuck-Muller, C. M., Chen, H., Martinez, J. E. és mtsai: Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature. Hum. Genet., 1995, 96, 119-129.
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Tuck-Muller, C. M., Chen, H., Martinez, J. E. és mtsai: Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature. Hum. Genet., 1995, 96, 119-129.
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Weckworth, P. F., Johnson, H. W., Pantzar, J. T. és mtsai: Dicentric Y chromosome and mixed dysgenesis. J. Urol., 1988, 139, 91-94.
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Weckworth, P. F., Johnson, H. W., Pantzar, J. T. és mtsai: Dicentric Y chromosome and mixed dysgenesis. J. Urol., 1988, 139, 91-94.
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