| scholarly article | Q13442814 |
| P50 | author | Megan Allyse | Q48107057 |
| Sharron Close | Q85284048 | ||
| Kirsten A Riggan | Q90268042 | ||
| P2860 | cites work | A review of trisomy X (47,XXX) | Q21093168 |
| Klinefelter syndrome and other sex chromosomal aneuploidies | Q21093172 | ||
| 48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome | Q24608052 | ||
| Dosage effects of X and Y chromosomes on language and social functioning in children with supernumerary sex chromosome aneuploidies: implications for idiopathic language impairment and autism spectrum disorders | Q24623933 | ||
| Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review | Q24649106 | ||
| 47,XYY syndrome: clinical phenotype and timing of ascertainment | Q33900758 | ||
| Diagnosis and mortality in 47,XYY persons: a registry study. | Q33930723 | ||
| Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities | Q34138636 | ||
| Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study | Q34175866 | ||
| Criminality in men with Klinefelter's syndrome and XYY syndrome: a cohort study. | Q34256362 | ||
| Increased mortality in Klinefelter syndrome. | Q34338468 | ||
| 47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling | Q34426883 | ||
| Morbidity in Klinefelter syndrome: a Danish register study based on hospital discharge diagnoses | Q34563913 | ||
| Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group | Q34574609 | ||
| Klinefelter syndrome in clinical practice | Q34616801 | ||
| Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY | Q35947200 | ||
| Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome | Q35972410 | ||
| Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features. | Q36589177 | ||
| The spectrum of the behavioral phenotype in boys and adolescents 47,XXY (Klinefelter syndrome). | Q37087992 | ||
| What parents are told after prenatal diagnosis of a sex chromosome abnormality: interview and questionnaire study | Q37129486 | ||
| The cognitive phenotype in Klinefelter syndrome: a review of the literature including genetic and hormonal factors | Q37656038 | ||
| Morbidity and mortality in Klinefelter syndrome (47,XXY). | Q37854088 | ||
| Decision to abort after a prenatal diagnosis of sex chromosome abnormality: a systematic review of the literature | Q37975107 | ||
| Neurocognitive variance and neurological underpinnings of the X and Y chromosomal variations | Q38075502 | ||
| Cognitive and neurological aspects of sex chromosome aneuploidies | Q38189893 | ||
| Attitudes and Knowledge of Maternal-Fetal Medicine Fellows Regarding Noninvasive Prenatal Testing. | Q38449983 | ||
| Cell-free DNA screening and sex chromosome aneuploidies | Q38531631 | ||
| Health-care provider communication with expectant parents during a prenatal diagnosis: an integrative review | Q38832382 | ||
| Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome. | Q38900036 | ||
| Parents' perspectives on the unforeseen finding of a fetal sex chromosomal aneuploidy | Q39786448 | ||
| Utilization of noninvasive prenatal testing: impact on referrals for diagnostic testing | Q41060187 | ||
| Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY. | Q41905132 | ||
| Mothers of children with Down syndrome reflect on their postnatal support | Q42644181 | ||
| Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system | Q43868192 | ||
| Socioeconomic trajectories affect mortality in Klinefelter syndrome. | Q44447897 | ||
| Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYY. | Q44745976 | ||
| Klinefelter syndrome: expanding the phenotype and identifying new research directions | Q47388441 | ||
| Parental experiences after prenatal diagnosis of fetal abnormality | Q47773163 | ||
| The use of noninvasive prenatal testing in obstetric care: educational resources, practice patterns, and barriers reported by a national sample of clinicians | Q47795103 | ||
| Tetrasomy and pentasomy of the X chromosome. | Q51462172 | ||
| Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis. | Q52848297 | ||
| Counseling parents before prenatal diagnosis: do we need to say more about the sex chromosome aneuploidies? | Q53087139 | ||
| The prevalence and diagnosis rates of Klinefelter syndrome: an Australian comparison. | Q53156189 | ||
| Mortality and incidence in women with 47,XXX and variants. | Q53180061 | ||
| Timing of diagnosis of 47,XXY and 48,XXYY: a survey of parent experiences. | Q55317666 | ||
| Socio-economic factors affect mortality in 47,XYY syndrome-A comparison with the background population and Klinefelter syndrome | Q57632069 | ||
| Health professionals' reports of information given to parents following the prenatal diagnosis of sex chromosome anomalies and outcomes of pregnancies: a pilot study | Q57745515 | ||
| Outcomes of pregnancies diagnosed with Klinefelter syndrome: the possible influence of health professionals†| Q57745536 | ||
| Language phenotypes in children with sex chromosome trisomies. | Q61660413 | ||
| Decisions following the intrauterine diagnosis of sex chromosome aneuploidy | Q69446380 | ||
| Genetic counseling for sex chromosome abnormalities | Q74457722 | ||
| What's the harm? Genetic counselor perceptions of adverse effects of genetics service provision by non-genetics professionals | Q86931900 | ||
| A first look at women's perspectives on noninvasive prenatal testing to detect sex chromosome aneuploidies and microdeletion syndromes | Q86978025 | ||
| Maternal age trends support uptake of non-invasive prenatal testing (NIPT) in the low-risk population | Q89168684 | ||
| Behavioral and psychological features in girls and women with triple-X syndrome | Q90710238 | ||
| Births in the United States, 2017 | Q91196725 | ||
| Speech and language in children with Klinefelter syndrome | Q92045374 | ||
| Cognitive Profile, Emotional-Behavioral Features, and Parental Stress in Boys With 47,XYY Syndrome | Q92791490 | ||
| Delivering the Diagnosis of Sex Chromosome Aneuploidy: Experiences and Preferences of Parents and Individuals | Q95363493 | ||
| P577 | publication date | 2020-03-17 | |
| P1433 | published in | American Journal of Medical Genetics Part C: Seminars in Medical Genetics | Q15749239 |
| P1476 | title | Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child |
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