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Maternal and Child Health Journal|September 3, 2013
Likelihood of emergency contraception use among African-American women at risk of adverse birth outcomesCatherine E Lind, Emily M Godfrey, Kristin M Rankin, et al.
The American Journal of Physiology|July 1, 1986
Porous-bottom dishes for culture of polarized cellsR E Steele, A S Preston, J P Johnson, et al.
The American Journal of Physiology|June 1, 1982
Aldosterone and corticosterone binding and effects on Na+ transport in cultured kidney cellsC O Watlington, F M Perkins, P J Munson, et al.
American Journal of Obstetrics and Gynecology|March 1, 1994
The relationship between exposure during pregnancy to cigarette smoking and cocaine use and placenta previaA S Handler, E D Mason, D L Rosenberg, et al.
The Journal of Membrane Biology|January 1, 1987
Isolation and characterization of specialized regions of toad urinary bladder apical plasma membrane involved in the water permeability response to antidiuretic hormoneH W Harris, H R Murphy, M C Willingham, et al.
Molecular Endocrinology (Baltimore, Md.)|May 1, 1991
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency alleleM T Tusie-Luna, P W Speiser, M Dumic, et al.
Thrombosis and Haemostasis|December 7, 1992
Recurrent, isolated factor X deficiency in myeloma: repeated normalization of factor X levels after cytostatic chemotherapy followed by late treatment failure associated with the development of systemic amyloidosisI Schwarzinger, M Stain-Kos, P Bettelheim, et al.
Molecular Genetics and Metabolism|November 14, 2000
A multicenter study of women with nonclassical congenital adrenal hyperplasia: relationship between genotype and phenotypeP W Speiser, E S Knochenhauer, D Dewailly, et al.
American Journal of Human Genetics|September 1, 1988
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequenciesC E Aston, S L Sherman, N E Morton, et al.
Recent Progress in Hormone Research|January 1, 1994
Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridizationP W Speiser, P C White, J Dupont, et al.
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