First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)

P. W. Speiser; N. Laforgia; K. Kato; J. Pareira; R. Khan; S. Y. Yang; C. Whorwood; P. C. White; S. Elias; E. Schriock; E. Schriock; J. L. Simpson; M. Taslimi; J. Najjar; S. May; G. Mills; C. Crawford; M. I. New

doi:10.1097/00006254-199010000-00020

First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)

P. W. Speiser, N. Laforgia, K. Kato, J. Pareira, R. Khan, S. Y. Yang, C. Whorwood, P. C. White, S. Elias, E. Schriock, E. Schriock, J. L. Simpson, M. Taslimi, J. Najjar, S. May, G. Mills, C. Crawford, M. I. New

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

Original language	English (US)
Pages (from-to)	707-709
Number of pages	3
Journal	Obstetrical and Gynecological Survey
Volume	45
Issue number	10
DOIs	https://doi.org/10.1097/00006254-199010000-00020
State	Published - Oct 1990

ASJC Scopus subject areas

Obstetrics and Gynecology

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10.1097/00006254-199010000-00020

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Speiser, P. W., Laforgia, N., Kato, K., Pareira, J., Khan, R., Yang, S. Y., Whorwood, C., White, P. C., Elias, S., Schriock, E., Schriock, E., Simpson, J. L., Taslimi, M., Najjar, J., May, S., Mills, G., Crawford, C., & New, M. I. (1990). First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency). Obstetrical and Gynecological Survey, 45(10), 707-709. https://doi.org/10.1097/00006254-199010000-00020

Speiser, PW, Laforgia, N, Kato, K, Pareira, J, Khan, R, Yang, SY, Whorwood, C, White, PC, Elias, S, Schriock, E, Schriock, E, Simpson, JL, Taslimi, M, Najjar, J, May, S, Mills, G, Crawford, C & New, MI 1990, 'First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)', Obstetrical and Gynecological Survey, vol. 45, no. 10, pp. 707-709. https://doi.org/10.1097/00006254-199010000-00020

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author = "Speiser, {P. W.} and N. Laforgia and K. Kato and J. Pareira and R. Khan and Yang, {S. Y.} and C. Whorwood and White, {P. C.} and S. Elias and E. Schriock and E. Schriock and Simpson, {J. L.} and M. Taslimi and J. Najjar and S. May and G. Mills and C. Crawford and New, {M. I.}",

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AU - Speiser, P. W.

AU - Laforgia, N.

AU - Kato, K.

AU - Pareira, J.

AU - Khan, R.

AU - Yang, S. Y.

AU - Whorwood, C.

AU - White, P. C.

AU - Elias, S.

AU - Schriock, E.

AU - Simpson, J. L.

AU - Taslimi, M.

AU - Najjar, J.

AU - May, S.

AU - Mills, G.

AU - Crawford, C.

AU - New, M. I.

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First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)

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