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

Phyllis W. Speiser; Nicola Laforgia; Koji Kato; Judith Pareira; Rafiya Khan; Soo Young Yang; Christopher Whorwood; Perrin C. White; Sherman Elias; Elizabeth Schriock; Eldon Schriock; Joe Leigh Simpson; Mark Taslimi; Jennifer Najjar; Steven May; Gary Mills; Christopher Crawford; Maria I. New

doi:10.1097/00006254-199010000-00020

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

Phyllis W. Speiser, Nicola Laforgia, Koji Kato, Judith Pareira, Rafiya Khan, Soo Young Yang, Christopher Whorwood, Perrin C. White, Sherman Elias, Elizabeth Schriock, Eldon Schriock, Joe Leigh Simpson, Mark Taslimi, Jennifer Najjar, Steven May, Gary Mills, Christopher Crawford, Maria I. New

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

Original language	English
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
Externally published	Yes

Access to Document

10.1097/00006254-199010000-00020

Cite this

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

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

author = "Speiser, {Phyllis W.} and Nicola Laforgia and Koji Kato and Judith Pareira and Rafiya Khan and Yang, {Soo Young} and Christopher Whorwood and White, {Perrin C.} and Sherman Elias and Elizabeth Schriock and Eldon Schriock and Simpson, {Joe Leigh} and Mark Taslimi and Jennifer Najjar and Steven May and Gary Mills and Christopher Crawford and New, {Maria I.}",

year = "1990",

month = oct,

doi = "10.1097/00006254-199010000-00020",

language = "English",

volume = "45",

pages = "707--709",

journal = "Obstetrical and Gynecological Survey",

issn = "0029-7828",

publisher = "Lippincott Williams and Wilkins Ltd.",

number = "10",

}

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

TY - JOUR

T1 - First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)

AU - Speiser, Phyllis W.

AU - Laforgia, Nicola

AU - Kato, Koji

AU - Pareira, Judith

AU - Khan, Rafiya

AU - Yang, Soo Young

AU - Whorwood, Christopher

AU - White, Perrin C.

AU - Elias, Sherman

AU - Schriock, Elizabeth

AU - Schriock, Eldon

AU - Simpson, Joe Leigh

AU - Taslimi, Mark

AU - Najjar, Jennifer

AU - May, Steven

AU - Mills, Gary

AU - Crawford, Christopher

AU - New, Maria I.

PY - 1990/10

Y1 - 1990/10

UR - http://www.scopus.com/inward/record.url?scp=0025045294&partnerID=8YFLogxK

U2 - 10.1097/00006254-199010000-00020

DO - 10.1097/00006254-199010000-00020

M3 - Article

AN - SCOPUS:0025045294

SN - 0029-7828

VL - 45

SP - 707

EP - 709

JO - Obstetrical and Gynecological Survey

JF - Obstetrical and Gynecological Survey

IS - 10

ER -