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Translocation (4;14) and concomitant inv(14) in a basal cell carcinoma

Universidade Estadual Paulista (Unesp) (1991-12-01)

Chromosome analysis of short-term cultures from a basal cell carcinoma was performed. The analyzed karyotypes showed a pseudodiploid clone characterized by a der(4)t(4;14)(p14;p11) and a concomitant inversion of the same ...

Tetrasomy 15Q11-Q13 identified by fluorescence in situ hybridization in a patient with autistic disorder

Silva, Ana Elizabete; Vayego-Lourenço, Sheila Adami; Fett-Conte, Agnes Cristina; Goloni-Bertollo, Eny Maria; Varella-Garcia, Marileila (2014)

Three Dinucleotide Markers On Chromosome 21.

de Souza, A P; Allamand, V; Richard, I; Brenguier, L; Beckmann, J S (1994)

Two Cases Of Y; Autosome Translocations: A 45,x Male And A Clinically Trisomy 18 Patient.

Farah, S B; Ramos, C F; de Mello, M P; Sartorato, E L; Horelli-Kuitunen, N; Lopes, V L; Cavalcanti, D P; Hackel, C (1994)

Interstitial long-arm deletion of chromosome 7 and ectrodactyly

Universidade Estadual Paulista (Unesp) (1989-01-01)

An interstitial deletion of 7q21 was found in a boy with mental retardation, microcephaly, convergent strabismus, micrognathia, genital anomalies, and other findings, including ectrodactyly.

Velocardiofacial syndrome with a rare t(2;22)

Universidade de São Paulo (USP); Universidade Estadual Paulista (Unesp) (2007-07-01)

Rearrangements involving chromosomes 2 and 22 were described not only as acquired abnormalities in a variety of human neoplasias but also in the constitutional karyotype suggesting the existence of a greater fragility in ...

Velocardiofacial syndrome with a rare t(2;22)

Huber, Jair; Rainho, Claudia A.; Gomes, Marcus V.; Santos, Silvio A.; Ramos, Ester S. (2014)

A rare non-Robertsonian translocation involving chromosomes 15 and 21

Universidade Estadual Paulista (Unesp); Universidade de São Paulo (USP) (Associação Paulista de Medicina (APM), 2013)

CONTEXTO:Translocações robertsonianas (TR) estão entre os rearranjos estruturais balanceados mais comuns em humanos e compreendem a fusão da cromatina completa do braço longo de dois cromossomos acrocêntricos. No entanto, ...

Translocation (4;14) and concomitant inv(14) in a basal cell carcinoma

Kawasaki, R. S.; Caldeira, L. F.; Andre, F. S.; Gasques, J. A L; Castilho, W. H.; Bozola, A. R.; Thome, J. A.; Tajara, E. H. (2014)

Partial Monosomy 21 (q11.2→q21.3) Combined With 3p25.3→pter Monosomy Due To An Unbalanced Translocation In A Patient Presenting Dysmorphic Features And Developmental Delay.

dos Santos, Ana Paula; Vieira, Társis Paiva; Simioni, Milena; Monteiro, Fabíola Paoli; Gil-da-Silva-Lopes, Vera Lúcia (2013)

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Translocation (4;14) and concomitant inv(14) in a basal cell carcinoma

Tetrasomy 15Q11-Q13 identified by fluorescence in situ hybridization in a patient with autistic disorder

Three Dinucleotide Markers On Chromosome 21.

Two Cases Of Y; Autosome Translocations: A 45,x Male And A Clinically Trisomy 18 Patient.

Interstitial long-arm deletion of chromosome 7 and ectrodactyly

Velocardiofacial syndrome with a rare t(2;22)

Velocardiofacial syndrome with a rare t(2;22)

A rare non-Robertsonian translocation involving chromosomes 15 and 21

Translocation (4;14) and concomitant inv(14) in a basal cell carcinoma

Partial Monosomy 21 (q11.2→q21.3) Combined With 3p25.3→pter Monosomy Due To An Unbalanced Translocation In A Patient Presenting Dysmorphic Features And Developmental Delay.