Partial trisomy 16 and genitourinary anomalies (2007)
- Authors:
- USP affiliated authors: MARTELLI, LUCIA REGINA - FMRP ; RAMOS, ESTER SILVEIRA - FMRP
- Unidade: FMRP
- Subjects: MALFORMAÇÕES; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: Annual Meeting of the American Society of Human Genetics (ASHG)
-
ABNT
BARATELA, W. A. R. et al. Partial trisomy 16 and genitourinary anomalies. 2007, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2007. . Acesso em: 14 fev. 2026. -
APA
Baratela, W. A. R., Martelli, L. R., Squire, J. A., Rebelo, C. C., Huber, J., Laureano, L. A. F., & Ramos, E. S. (2007). Partial trisomy 16 and genitourinary anomalies. In Abstracts. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Baratela WAR, Martelli LR, Squire JA, Rebelo CC, Huber J, Laureano LAF, Ramos ES. Partial trisomy 16 and genitourinary anomalies. Abstracts. 2007 ;[citado 2026 fev. 14 ] -
Vancouver
Baratela WAR, Martelli LR, Squire JA, Rebelo CC, Huber J, Laureano LAF, Ramos ES. Partial trisomy 16 and genitourinary anomalies. Abstracts. 2007 ;[citado 2026 fev. 14 ] - XX/XY chimerism in male infertility
- Familial translocation t(3;10)(p26; p11.2) involving four generations and leading to a partial trisomy 10p and monosomy 3q
- A distinct phenotype of ring chromosome 4
- Phenotype karyotype correlation in a patient with interstitial deletion 11q
- Variante da Síndrome Ullrich-Turner e Neurofibromatose Tipo I
- Phenotypic abnormalities in a familial translocation (11,18) (q231, q12.2)
- Síndrome velo-cardio-facial por translocação (2;22)
- Case report: patient with ring chromosome 4
- Effectiveness of comprehensive cytogenetic investigations in the diagnosis and genetic counseling of 8,131 patients
- Submicroscopic deletions analysis in chromosome 22q11.2 in 11 families with velocardiofacial syndrome patients
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas