يعرض 1 - 2 نتائج من 2 نتيجة بحث عن '"chromosome deletion 22q11/cn [Congenital Disorder]"', وقت الاستعلام: 0.34s تنقيح النتائج
  1. 1
    Electronic Resource

    مصطلحات الفهرس: monosomy X/di [Diagnosis], perinatal period, polyploidy, population research, prenatal diagnosis, prenatal period, prevalence, sex chromosome aberration/cn [Congenital Disorder], sex chromosome aberration/di [Diagnosis], spontaneous abortion, stillbirth, trisomy/cn [Congenital Disorder], trisomy/di [Diagnosis], trisomy 13/cn [Congenital Disorder], trisomy 13/di [Diagnosis], trisomy 16/cn [Congenital Disorder], trisomy 16/di [Diagnosis], trisomy 18/cn [Congenital Disorder], trisomy 18/di [Diagnosis], trisomy 21/cn [Congenital Disorder], trisomy 21/di [Diagnosis], DNA/ec [Endogenous Compound], trisomy 15/cn [Congenital Disorder], trisomy 15/di [Diagnosis], trisomy 22/cn [Congenital Disorder], trisomy 22/di [Diagnosis], article, 47,XXY syndrome/cn [Congenital Disorder], 47,XXY syndrome/di [Diagnosis], adult, amniocentesis, chorion villus sampling, chromosome aberration/cn [Congenital Disorder], chromosome aberration/di [Diagnosis], chromosome analysis, chromosome deletion 22q11/cn [Congenital Disorder], chromosome deletion 22q11/di [Diagnosis], cohort analysis, congenital malformation/cn [Congenital Disorder], controlled study, copy number variation, developmental stage, diagnostic value, female, fetus disease/cn [Congenital Disorder], fetus disease/di [Diagnosis], fetus echography, first trimester pregnancy, gene frequency, genetic screening, gestational age, heart disease/cn [Congenital Disorder], heart disease/di [Diagnosis], human, infant, live birth, major clinical study, maternal age, monosomy X/cn [Congenital Disorder], Article

    URL: https://repository.monashhealth.org/monashhealthjspui/handle/1/29241
    Human Reproduction
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  2. 2
    Electronic Resource

    مصطلحات الفهرس: monosomy X/di [Diagnosis], perinatal period, polyploidy, population research, prenatal diagnosis, prenatal period, prevalence, sex chromosome aberration/cn [Congenital Disorder], sex chromosome aberration/di [Diagnosis], spontaneous abortion, stillbirth, trisomy/cn [Congenital Disorder], trisomy/di [Diagnosis], trisomy 13/cn [Congenital Disorder], trisomy 13/di [Diagnosis], trisomy 16/cn [Congenital Disorder], trisomy 16/di [Diagnosis], trisomy 18/cn [Congenital Disorder], trisomy 18/di [Diagnosis], trisomy 21/cn [Congenital Disorder], trisomy 21/di [Diagnosis], DNA/ec [Endogenous Compound], trisomy 15/cn [Congenital Disorder], trisomy 15/di [Diagnosis], trisomy 22/cn [Congenital Disorder], trisomy 22/di [Diagnosis], article, 47,XXY syndrome/cn [Congenital Disorder], 47,XXY syndrome/di [Diagnosis], adult, amniocentesis, chorion villus sampling, chromosome aberration/cn [Congenital Disorder], chromosome aberration/di [Diagnosis], chromosome analysis, chromosome deletion 22q11/cn [Congenital Disorder], chromosome deletion 22q11/di [Diagnosis], cohort analysis, congenital malformation/cn [Congenital Disorder], controlled study, copy number variation, developmental stage, diagnostic value, female, fetus disease/cn [Congenital Disorder], fetus disease/di [Diagnosis], fetus echography, first trimester pregnancy, gene frequency, genetic screening, gestational age, heart disease/cn [Congenital Disorder], heart disease/di [Diagnosis], human, infant, live birth, major clinical study, maternal age, monosomy X/cn [Congenital Disorder], Article