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 journalArticle

Original languageEnglish (US)
Pages (from-to)707-709
Number of pages3
JournalObstetrical and Gynecological Survey
Volume45
Issue number10
StatePublished - 1990

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Congenital Adrenal Hyperplasia
First Pregnancy Trimester
Molecular Biology
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

ASJC Scopus subject areas

  • Obstetrics and Gynecology

Cite this

Speiser, P. W., Laforgia, N., Kato, K., Pareira, J., Khan, R., Yang, S. Y., ... 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.

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

In: Obstetrical and Gynecological Survey, Vol. 45, No. 10, 1990, p. 707-709.

Research output: Contribution to journalArticle

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.
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. / First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency). In: Obstetrical and Gynecological Survey. 1990 ; Vol. 45, No. 10. pp. 707-709.
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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 - 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.

PY - 1990

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JO - Obstetrical and Gynecological Survey

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