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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)

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

Velocardiofacial syndrome with a rare t(2;22)

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

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.

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)

Dna Content, Chromatin Texture And Nuclear Morphology In Benzo[a]pyrene-transformed Human Breast Epithelial Cells After Microcell-mediated Transfer Of Chromosomes 11 And 17.

Mello, Maria Luiza S; de Campos Vidal, Benedicto; Lareef, Mohamed H; Hu, Yun F; Yang, Xiaoqi; Russo, Jose (2003)

Investigation Of The 22q11.2 Candidate Region In Patients With Midline Facial Defects With Hypertelorism.

Simioni, M; Freitas, E Lopes; Vieira, T Paiva; Lopes-Cendes, I; Gil-da-Silva-Lopes, V Lúcia (2010)

Allelic Imbalance Studies Of Chromosome 9 Suggest Major Differences In Chromosomal Instability Among Nonmelanoma Skin Carcinomas.

Gomes, Gabriela Pereira; Moraes, Aparecida Machado; Stoff, Hamilton Ometto; Ward, Laura Sterian (2004)

Attention-deficit/hyperactivity disorder in a population isolate : linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11

Arcos Burgos, Oscar Mauricio; Castellanos, Francisco Xavier; Pineda Salazar, David Antonio; Lopera Restrepo, Francisco Javier; Palacio Ortiz, Juan David; Palacio Baena, Luis Guillermo; Rapoport, Judith; Berg, Kate; Bailey Wilson, Joan E.; Muenke, Maximilian (Cell PressGenética Regeneración y CáncerGrupo de Neurociencias de AntioquiaGrupo Neuropsicología y ConductaBaltimore, Estados Unidos, 2022)

Genomic Imbalances Detected Through Array Cgh In Fetuses With Holoprosencephaly.

Machado, Isabela Nelly; Heinrich, Juliana Karina; Barini, Ricardo (2011)

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Velocardiofacial syndrome with a rare t(2;22)

Velocardiofacial syndrome with a rare t(2;22)

Velocardiofacial syndrome with a rare t(2;22)

Interstitial long-arm deletion of chromosome 7 and ectrodactyly

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

Dna Content, Chromatin Texture And Nuclear Morphology In Benzo[a]pyrene-transformed Human Breast Epithelial Cells After Microcell-mediated Transfer Of Chromosomes 11 And 17.

Investigation Of The 22q11.2 Candidate Region In Patients With Midline Facial Defects With Hypertelorism.

Allelic Imbalance Studies Of Chromosome 9 Suggest Major Differences In Chromosomal Instability Among Nonmelanoma Skin Carcinomas.

Attention-deficit/hyperactivity disorder in a population isolate : linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11

Genomic Imbalances Detected Through Array Cgh In Fetuses With Holoprosencephaly.