Timing of diagnosis of 47,XXY and 48,XXYY: A survey of parent experiences
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference17 articles.
1. 47,XXY (Klinefelter syndrome) and 47,XYY: Estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling;Abramsky;Prenat Diagn,1997
2. Dyslexia in 47,XXY boys identified at birth;Bender;Behav Genet,1986
3. Prenatal and postnatal prevalence of Klinefelter syndrome: A national registry study;Bojesen;J Clin Endocrinol Metab,2003
4. Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA;Coffee;Am J Hum Genet,2009
5. Oral and written language abilities of XXY boys: Implications for anticipatory guidance;Graham;Pediatrics,1988
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3. OSTEOPOROTIC FRACTURES AND 48XXYY SYNDROME: CLINICAL CASE;Revista Portuguesa de Endocrinologia, Diabetes e Metabolismo;2023
4. “Knowledge is Power”: Parent Views on the Benefits of Early Diagnosis and Awareness of Sex Chromosome Multisomy Among Pediatric Professionals;Journal of Developmental & Behavioral Pediatrics;2022-11-30
5. Respecting Autonomy and Balancing Benefits by Disclosing the Secondary Finding of Klinefelter’s;The American Journal of Bioethics;2022-09-28
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