Deletion of the short arm of chromosome 20 (1987)
- Authors:
- USP affiliated authors: MORGANTE, ANGELA MARIA VIANNA - IB ; COSTA, ANTONIO RICHIERI DA - HRAC
- Unidades: IB; HRAC
- DOI: 10.1111/j.1399-0004.1987.tb02833.x
- Subjects: DELEÇÃO DE GENES; ANORMALIDADES MÚLTIPLAS
- Language: Português
- Imprenta:
- Source:
- Título do periódico: Clinical Genetics
- Volume/Número/Paginação/Ano: v.31, n.6 , p.406-9, jun. 1987
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
VIANNA-MORGANTE, Angela Maria; RICHIERI-COSTA, A; ROSENBERG, C. Deletion of the short arm of chromosome 20. Clinical Genetics, New York, v. 31, n. ju 1987, p. 406-9, 1987. DOI: 10.1111/j.1399-0004.1987.tb02833.x. -
APA
Vianna-Morgante, A. M., Richieri-Costa, A., & Rosenberg, C. (1987). Deletion of the short arm of chromosome 20. Clinical Genetics, 31( ju 1987), 406-9. doi:10.1111/j.1399-0004.1987.tb02833.x -
NLM
Vianna-Morgante AM, Richieri-Costa A, Rosenberg C. Deletion of the short arm of chromosome 20. Clinical Genetics. 1987 ;31( ju 1987): 406-9. -
Vancouver
Vianna-Morgante AM, Richieri-Costa A, Rosenberg C. Deletion of the short arm of chromosome 20. Clinical Genetics. 1987 ;31( ju 1987): 406-9. - Duplication of distal 17q: report of an observation [Brief clinical report]
- Tetrasomy 18p: tentative delineation of a syndrome
- Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome
- Sindrome fg associada com a mutacao da sindrome do cromossomo x fragil
- Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents
- Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents
- Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrom
- Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling
- Subtelomeric investigation in individuals with microform of HPE
- Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome
Informações sobre o DOI: 10.1111/j.1399-0004.1987.tb02833.x (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas