Optimising management in Turner syndrome: from infancy to adult transfer

التفاصيل البيبلوغرافية
العنوان:	Optimising management in Turner syndrome: from infancy to adult transfer
المؤلفون:	Donaldson, M D C, Gault, E J, Tan, K W, Dunger, D B
بيانات النشر:	BMJ Publishing Group Ltd
سنة النشر:	2006
المجموعة:	HighWire Press (Stanford University)
مصطلحات موضوعية:	Reviews
الوصف:	Turner syndrome can be defined as loss or abnormality of the second X chromosome in at least one cell line in a phenotypic female. The condition occurs in approximately 1 in every 2000 live female births,1 so that in the UK the prevalence for any year of life is in the region of 200 girls. The condition is much more common in utero, it being estimated that 1–2% of all conceptuses are affected, of whom only 1% will survive to term.2,3
نوع الوثيقة:	text
وصف الملف:	text/html
اللغة:	English
Relation:	http://adc.bmj.com/cgi/content/short/91/6/513; http://dx.doi.org/10.1136/adc.2003.035907
DOI:	10.1136/adc.2003.035907
الاتاحة:	http://adc.bmj.com/cgi/content/short/91/6/513 https://doi.org/10.1136/adc.2003.035907
Rights:	Copyright (C) 2006, BMJ Publishing Group Ltd
رقم الانضمام:	edsbas.3015A65C
قاعدة البيانات:	BASE

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