Prenatal diagnosis of fragile X syndrome

Mark Hirst; Samantha Knight; Kay Davies; Gareth Cross; Kevin Ocraft; Sandy Raeburn; Shauna Heeger; Deborah Eunpu; Edmund C. Jenkins; Richard Lindenbaum; Carl S. Dobkin; Xiao Hua Ding; Edmund C. Jenkins; Michael S. Krawczun; W. Ted Brown; Ponmani Goonewardena; Judy Willner; Cindy Benson; Dominique Heitz; Francois Rousseau

doi:10.1016/0140-6736(91)91831-E

Prenatal diagnosis of fragile X syndrome

Mark Hirst
, Samantha Knight
, Kay Davies
, Gareth Cross
, Kevin Ocraft
, Sandy Raeburn
, Shauna Heeger
, Deborah Eunpu
, Edmund C. Jenkins
, Richard Lindenbaum
, Carl S. Dobkin
, Xiao Hua Ding
, Edmund C. Jenkins
, Michael S. Krawczun
, W. Ted Brown
, Ponmani Goonewardena
, Judy Willner
, Cindy Benson
, Dominique Heitz
, Francois Rousseau

Friedman Brain Institute

Research output: Contribution to journal › Letter › peer-review

18 Scopus citations

Original language	English
Pages (from-to)	956-958
Number of pages	3
Journal	The Lancet
Volume	338
Issue number	8772
DOIs	https://doi.org/10.1016/0140-6736(91)91831-E
State	Published - 12 Oct 1991

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10.1016/0140-6736(91)91831-E

Cite this

Hirst, M., Knight, S., Davies, K., Cross, G., Ocraft, K., Raeburn, S., Heeger, S., Eunpu, D., Jenkins, E. C., Lindenbaum, R., Dobkin, C. S., Ding, X. H., Jenkins, E. C., Krawczun, M. S., Ted Brown, W., Goonewardena, P., Willner, J., Benson, C., Heitz, D., & Rousseau, F. (1991). Prenatal diagnosis of fragile X syndrome. The Lancet, 338(8772), 956-958. https://doi.org/10.1016/0140-6736(91)91831-E

@article{661fa2bf36b94ab8bb635feba0f2b655,

title = "Prenatal diagnosis of fragile X syndrome",

author = "Mark Hirst and Samantha Knight and Kay Davies and Gareth Cross and Kevin Ocraft and Sandy Raeburn and Shauna Heeger and Deborah Eunpu and Jenkins, \{Edmund C.\} and Richard Lindenbaum and Dobkin, \{Carl S.\} and Ding, \{Xiao Hua\} and Jenkins, \{Edmund C.\} and Krawczun, \{Michael S.\} and \{Ted Brown\}, W. and Ponmani Goonewardena and Judy Willner and Cindy Benson and Dominique Heitz and Francois Rousseau",

note = "Funding Information: Dr Ian Young counselled family B during prenatal testing. This work was funded by the Medical Research Council and Action Research for the Funding Information: Crippled Child, and was partly supported by grant MCJ360587 from the Maternal and Child Health Program, US Department of Health and Human Services. Funding Information: This work has been supported in part by AIRC. Funding Information: We thank the cytogenetic technological staff at the Institute for Basic Research for their help in this study. Partial support for these studies was provided by the New York State Office of Mental Retardation and Developmental Disabilities and by grant MCJ36058702 from the Bureau of Maternal and Child Health.",

year = "1991",

month = oct,

day = "12",

doi = "10.1016/0140-6736(91)91831-E",

language = "English",

volume = "338",

pages = "956--958",

journal = "The Lancet",

issn = "0140-6736",

publisher = "Elsevier B.V.",

number = "8772",

}

Hirst, M, Knight, S, Davies, K, Cross, G, Ocraft, K, Raeburn, S, Heeger, S, Eunpu, D, Jenkins, EC, Lindenbaum, R, Dobkin, CS, Ding, XH, Jenkins, EC, Krawczun, MS, Ted Brown, W, Goonewardena, P, Willner, J, Benson, C, Heitz, D & Rousseau, F 1991, 'Prenatal diagnosis of fragile X syndrome', The Lancet, vol. 338, no. 8772, pp. 956-958. https://doi.org/10.1016/0140-6736(91)91831-E

TY - JOUR

T1 - Prenatal diagnosis of fragile X syndrome

AU - Hirst, Mark

AU - Knight, Samantha

AU - Davies, Kay

AU - Cross, Gareth

AU - Ocraft, Kevin

AU - Raeburn, Sandy

AU - Heeger, Shauna

AU - Eunpu, Deborah

AU - Jenkins, Edmund C.

AU - Lindenbaum, Richard

AU - Dobkin, Carl S.

AU - Ding, Xiao Hua

AU - Jenkins, Edmund C.

AU - Krawczun, Michael S.

AU - Ted Brown, W.

AU - Goonewardena, Ponmani

AU - Willner, Judy

AU - Benson, Cindy

AU - Heitz, Dominique

AU - Rousseau, Francois

N1 - Funding Information: Dr Ian Young counselled family B during prenatal testing. This work was funded by the Medical Research Council and Action Research for the Funding Information: Crippled Child, and was partly supported by grant MCJ360587 from the Maternal and Child Health Program, US Department of Health and Human Services. Funding Information: This work has been supported in part by AIRC. Funding Information: We thank the cytogenetic technological staff at the Institute for Basic Research for their help in this study. Partial support for these studies was provided by the New York State Office of Mental Retardation and Developmental Disabilities and by grant MCJ36058702 from the Bureau of Maternal and Child Health.

PY - 1991/10/12

Y1 - 1991/10/12

UR - https://www.scopus.com/pages/publications/0026049556

U2 - 10.1016/0140-6736(91)91831-E

DO - 10.1016/0140-6736(91)91831-E

M3 - Letter

C2 - 1681307

AN - SCOPUS:0026049556

SN - 0140-6736

VL - 338

SP - 956

EP - 958

JO - The Lancet

JF - The Lancet

IS - 8772

ER -