Submicroscopic deletions analysis in chromosome 22q11.2 in 11 families with velocardiofacial syndrome patients (2000)
- Authors:
- USP affiliated authors: MARTELLI, LUCIA REGINA - FMRP ; RAMOS, ESTER SILVEIRA - FMRP
- Unidade: FMRP
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirão Preto
- Date published: 2000
- Source:
- Título: Genetics and Molecular Biology
- ISSN: 1415-4757
- Volume/Número/Paginação/Ano: v. 23, n. 3, supl., p. 586 res. GH080, 2000
- Conference titles: Congresso Nacional de Genética
-
ABNT
GARCIA, P. S. et al. Submicroscopic deletions analysis in chromosome 22q11.2 in 11 families with velocardiofacial syndrome patients. Genetics and Molecular Biology. Ribeirão Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 14 fev. 2026. , 2000 -
APA
Garcia, P. S., Martelli, L. R., Ramos, E. S., & Richieri-Costa, A. (2000). Submicroscopic deletions analysis in chromosome 22q11.2 in 11 families with velocardiofacial syndrome patients. Genetics and Molecular Biology. Ribeirão Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Garcia PS, Martelli LR, Ramos ES, Richieri-Costa A. Submicroscopic deletions analysis in chromosome 22q11.2 in 11 families with velocardiofacial syndrome patients. Genetics and Molecular Biology. 2000 ; 23( 3): 586 res. GH080.[citado 2026 fev. 14 ] -
Vancouver
Garcia PS, Martelli LR, Ramos ES, Richieri-Costa A. Submicroscopic deletions analysis in chromosome 22q11.2 in 11 families with velocardiofacial syndrome patients. Genetics and Molecular Biology. 2000 ; 23( 3): 586 res. GH080.[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
- Partial trisomy 16 and genitourinary anomalies
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