Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data (1999)
- Authors:
- Allingham-Hawkins, Diane J
- Babul-Hirji, Riyana
- Chitayat, David
- Holden, Jeanette J A
- Yang, Kathy T
- Lee, C
- Hudson, R
- Gorwill, H
- Nolin, Sarah L
- Glicksman, Anne
- Jenkins, Edmund C
- Brown, W Ted
- Howard-Peebles, Patricia N
- Becchi, Cindy
- Cummings, Emilie
- Fallon, Lee
- Seitz, Suzanne
- Black, Susan H
- Vianna-Morgante, Angela M

- Costa, Silvia S
- Otto, Paulo A

- Mingroni Netto, Regina Celia

- Murray, Anna
- Webb, J
- MacSwinney, F
- Dennis, N
- Jacobs, Patricia A
- Syrrou, Maria
- Georgiou, Ioannis
- Patsalis, Phillipos C
- Uzielli, Maria L Giovannucci
- Guarducci, S
- Lapi, E
- Cecconi, A
- Ricci, U
- Ricotti, G
- Biondi, C
- Scarselli, B
- Vieri, F
- USP affiliated authors: MORGANTE, ANGELA MARIA VIANNA - IB ; OTTO, PAULO ALBERTO - IB ; MINGRONI NETTO, REGINA CELIA - IB
- Unidade: IB
- DOI: 10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics
- ISSN: 0148-7299
- Volume/Número/Paginação/Ano: v. 83. n. 4, p. 322-325, apr., 1999
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ALLINGHAM-HAWKINS, Diane J et al. Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data. American Journal of Medical Genetics, v. 83. n. 4, p. 322-325, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b. Acesso em: 30 dez. 2025. -
APA
Allingham-Hawkins, D. J., Babul-Hirji, R., Chitayat, D., Holden, J. J. A., Yang, K. T., Lee, C., et al. (1999). Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data. American Journal of Medical Genetics, 83. n. 4, 322-325. doi:10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b -
NLM
Allingham-Hawkins DJ, Babul-Hirji R, Chitayat D, Holden JJA, Yang KT, Lee C, Hudson R, Gorwill H, Nolin SL, Glicksman A, Jenkins EC, Brown WT, Howard-Peebles PN, Becchi C, Cummings E, Fallon L, Seitz S, Black SH, Vianna-Morgante AM, Costa SS, Otto PA, Mingroni Netto RC, Murray A, Webb J, MacSwinney F, Dennis N, Jacobs PA, Syrrou M, Georgiou I, Patsalis PC, Uzielli MLG, Guarducci S, Lapi E, Cecconi A, Ricci U, Ricotti G, Biondi C, Scarselli B, Vieri F. Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data [Internet]. American Journal of Medical Genetics. 1999 ; 83. n. 4 322-325.[citado 2025 dez. 30 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b -
Vancouver
Allingham-Hawkins DJ, Babul-Hirji R, Chitayat D, Holden JJA, Yang KT, Lee C, Hudson R, Gorwill H, Nolin SL, Glicksman A, Jenkins EC, Brown WT, Howard-Peebles PN, Becchi C, Cummings E, Fallon L, Seitz S, Black SH, Vianna-Morgante AM, Costa SS, Otto PA, Mingroni Netto RC, Murray A, Webb J, MacSwinney F, Dennis N, Jacobs PA, Syrrou M, Georgiou I, Patsalis PC, Uzielli MLG, Guarducci S, Lapi E, Cecconi A, Ricci U, Ricotti G, Biondi C, Scarselli B, Vieri F. Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data [Internet]. American Journal of Medical Genetics. 1999 ; 83. n. 4 322-325.[citado 2025 dez. 30 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b - X-inactivation in fragile-X carriers
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- Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families
- Ectrodactilia associada à hemimelia tibial não segrega com marcadores dos cromossomos 7 e 10
- Premature ovarian failure (POF) in brazilian fragile X carriers
- Chromosome imbalances in syndromic hearing loss
- Distribution of CGG repeats and GRAXAC1/DXS548 alleles in south american populations
- Increased frequency of gray zone-premutated fraxa alleles in brazilian mentally impaired boys
Informações sobre o DOI: 10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b (Fonte: oaDOI API)
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