Complex chromosome rearrangement (CCR) involving chromosomes 2,5,11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verifled by spectra karyotyping (SKY) in a girl with mlld dysmorphic features and mental retardation (1999)
- Authors:
- USP affiliated authors: RAMOS, ESTER SILVEIRA - FMRP ; MARTELLI, LUCIA REGINA - FMRP
- Unidade: FMRP
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Human Genetics
- Volume/Número/Paginação/Ano: v. 65, n. 4, p. A356 res. 2009, 1999
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
RAMOS, Ester Silveira et al. Complex chromosome rearrangement (CCR) involving chromosomes 2,5,11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verifled by spectra karyotyping (SKY) in a girl with mlld dysmorphic features and mental retardation. American Journal of Human Genetics. Baltimore: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 19 set. 2024. , 1999 -
APA
Ramos, E. S., Rogatto, S. R., Martelli, L. R., Piram, S. A., & Squire, J. A. (1999). Complex chromosome rearrangement (CCR) involving chromosomes 2,5,11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verifled by spectra karyotyping (SKY) in a girl with mlld dysmorphic features and mental retardation. American Journal of Human Genetics. Baltimore: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Ramos ES, Rogatto SR, Martelli LR, Piram SA, Squire JA. Complex chromosome rearrangement (CCR) involving chromosomes 2,5,11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verifled by spectra karyotyping (SKY) in a girl with mlld dysmorphic features and mental retardation. American Journal of Human Genetics. 1999 ; 65( 4): A356 res. 2009.[citado 2024 set. 19 ] -
Vancouver
Ramos ES, Rogatto SR, Martelli LR, Piram SA, Squire JA. Complex chromosome rearrangement (CCR) involving chromosomes 2,5,11, and 16 and a reciprocal translocation between chromosomes 6 and 8 verifled by spectra karyotyping (SKY) in a girl with mlld dysmorphic features and mental retardation. American Journal of Human Genetics. 1999 ; 65( 4): A356 res. 2009.[citado 2024 set. 19 ] - Defeito diafragmático, espinha bífida, pé fendido: síndrome de Czeizel-Losonci?
- Diagnóstico de trissomia 13 e de aberração estrutural do cromossomo X na mesam irmandade
- Molecular cytogenetic characterization of an unbalanced t(4p;21q) in a patient misdiagnosed as full monosomy 21
- Correlação cariótipo-fenótipo de deleção terminal do cromossomo 2 (del 2q37.1)
- Submicroscopic deletions analysis in chromosome 22q11.2 in 11 families with velocardiofacial syndrome patients
- Detecção de seqüências Y-específicas em pacientes com alterações estruturais do cromossomo Y
- Partial trisomy 16 and genitourinary anomalies
- Protocolo de investigação citogenética para diagnóstico de cromossomos marcadores
- A distinct phenotype of ring chromosome 4
- XX/XY chimerism in male infertility
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
