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1 significantly associated with fecundability (time to pregnancy).
2 -dichloro-2,2-bis(p-chlorophenyl)ethylene to time to pregnancy.
3 llutants and couple fecundity as measured by time to pregnancy.
4 ter cycle length was associated with delayed time to pregnancy.
5 sh couples' fecundity, resulting in a longer time to pregnancy.
6 iation between menstrual characteristics and time to pregnancy among 2,653 Danish women enrolled in a
7 ercourse behavior can have a large impact on time to pregnancy and, likewise, on fecundability ratios
8 ion to follicular- and luteal-phase lengths, time to pregnancy, and early pregnancy loss (within 6 we
9 gths, discrete-time fecundability models for time to pregnancy, and logistic regression for early pre
10 association between PCB and DDE exposure and time to pregnancy by using serum levels measured in 390
11                                  Prospective time-to-pregnancy cohort study (2008 to date of last fol
12          Although survivors had an increased time to pregnancy compared with their siblings (p=0.032)
13 rall, DES was not associated with a delay in time to pregnancy (fecundability ratio = 0.95, 95% confi
14 eive, we found good fits to observed data on time to pregnancy for different populations.
15                                Compared with time to pregnancy for women in the lowest exposure categ
16                                  We recorded time to pregnancy in 289 eldest daughters 28-31 years la
17              We investigated infertility and time to pregnancy in female childhood cancer survivors,
18 re used to estimate fecundability ratios for time to pregnancy in relation to DES.
19 < 1.24 microg/liter, DDE < 14 microg/liter), time to pregnancy increased for women in the highest exp
20                                     Overall, time to pregnancy increased with increasing serum PCB le
21                       We recently found that time to pregnancy is prolonged in asthmatic females espe
22 renatal diethylstilbestrol (DES) exposure on time to pregnancy or secondary sex ratio in men.
23   All 3 approaches involve the collection of time-to-pregnancy or attempt-time data, and most are lim
24 ntal alterations in follicular-phase length, time to pregnancy, or early pregnancy loss, and in fact,
25                                       Unlike time to pregnancy, serum AMH level can be assessed regar
26 e available and therefore were excluded from time to pregnancy studies may now use oral contraceptive
27                                              Time to pregnancy studies seldom utilize detailed data o
28 aluate the effect of maternal age on waiting time to pregnancy, the authors reviewed hospital charts
29 s of 5 major European data sets with data on time to pregnancy (TTP) and proportion of contraceptive
30 als in the context of fecundity, measured as time to pregnancy (TTP).
31 f assessing biologic fertility is to measure time to pregnancy (TTP).
32     Biologic fertility can be measured using time to pregnancy (TTP).
33 sensitive functional measure of fertility is time to pregnancy (TTP); this can be studied retrospecti
34 in couple fertility was assessed by means of time to pregnancy (TTP--a sensitive and validated measur
35 sumption of contaminated fish in relation to time-to-pregnancy (TTP) among women in the New York Stat
36                                              Time to pregnancy, typically defined as the number of me
37  association between PCB or DDE exposure and time to pregnancy was weak and inconclusive.
38                The core measurement would be time to pregnancy, which can be carried out using a shor

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