Case report: patient with ring chromosome 4 (2007)
- Authors:
- USP affiliated authors: RAMOS, ESTER SILVEIRA - FMRP ; MARTELLI, LUCIA REGINA - FMRP
- Unidade: FMRP
- Subjects: ANORMALIDADES CROMOSSÔMICAS; CROMOSSOMOS HUMANOS
- Language: Inglês
- Imprenta:
- Source:
- Título: European Journal of Human Genetics
- ISSN: 1018-4813
- Volume/Número/Paginação/Ano: v. 15, suppl. 1, p. 122, res. P0397, 2007
- Conference titles: European Human Genetics Conference
-
ABNT
HUBER, J. et al. Case report: patient with ring chromosome 4. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 25 fev. 2026. , 2007 -
APA
Huber, J., Ramos, E. S., Melo, D. G., & Martelli, L. R. (2007). Case report: patient with ring chromosome 4. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Huber J, Ramos ES, Melo DG, Martelli LR. Case report: patient with ring chromosome 4. European Journal of Human Genetics. 2007 ; 15 122.[citado 2026 fev. 25 ] -
Vancouver
Huber J, Ramos ES, Melo DG, Martelli LR. Case report: patient with ring chromosome 4. European Journal of Human Genetics. 2007 ; 15 122.[citado 2026 fev. 25 ] - 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)
- Effectiveness of comprehensive cytogenetic investigations in the diagnosis and genetic counseling of 8,131 patients
- Partial trisomy 16 and genitourinary anomalies
- Submicroscopic deletions analysis in chromosome 22q11.2 in 11 families with velocardiofacial syndrome patients
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