Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly (2007)
- Authors:
- USP affiliated authors: RAMOS, ESTER SILVEIRA - FMRP ; MARTELLI, LUCIA REGINA - FMRP ; REIS, ROSANA MARIA DOS - FMRP
- Unidade: FMRP
- Subjects: ANORMALIDADES CROMOSSÔMICAS; SAÚDE DA MULHER
- Language: Inglês
- Imprenta:
- Source:
- Título: European Journal of Human Genetics
- ISSN: 1018-4813
- Volume/Número/Paginação/Ano: v. 15, suppl. 1, p. 92, res. P0260, 2007
- Conference titles: European Human Genetics Conference
-
ABNT
RAMOS, Ester Silveira et al. Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 11 fev. 2026. , 2007 -
APA
Ramos, E. S., Araújo, A., Martinhago, C. D., Martelli, L. R., Reis, R. M. dos, & Melo, D. G. (2007). Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Ramos ES, Araújo A, Martinhago CD, Martelli LR, Reis RM dos, Melo DG. Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly. European Journal of Human Genetics. 2007 ; 15 92.[citado 2026 fev. 11 ] -
Vancouver
Ramos ES, Araújo A, Martinhago CD, Martelli LR, Reis RM dos, Melo DG. Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly. European Journal of Human Genetics. 2007 ; 15 92.[citado 2026 fev. 11 ] - Correlation between chromossomal aneuploidy in sperm and embryo implantation rate
- Effect of varicocelectomy on spermatic global DNA methylation
- Filhos de pacientes com síndrome de Turner
- 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)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas