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 acesso aberto
- Este artigo NÃO é de acesso aberto
-
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: 18 fev. 2026. -
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 2026 fev. 18 ] 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 2026 fev. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b - Premature ovarian failure (POF) in brazilian fragile X carriers
- Premature ovarian failure (POF) in brazilian fragile X carriers
- Princípios de genética humana e médica
- 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
- Heterogeneidade genetica na ectrodactilia
- X-inactivation in fragile-X carriers
- Chromosome imbalances in syndromic hearing loss
- Fraxf in a patient with chromosome 8 duplication
- Distribuição das repetições CGG do loco FMR-1 e dos alelos dos microssatélites FRAXAC1/DXS548 em populações brasileiras
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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