Titlebook: Anorectal Malformations in Children; Embryology, Diagnosi Alexander M. Hohlschneider,John M. Hustson Book 20061st edition Springer-Verlag B

彎彎曲曲

compose

誘導(dǎo)

擴(kuò)大

責(zé)怪

NUDGE

https://doi.org/10.1007/978-3-663-05837-3 period of time become rare in the same part of the world at another period of time. Nevertheless, many varieties of ARM are seen universally and have been seen over several decades; these varieties merit the name “common” and will not be discussed in this chapter.

古文字學(xué)

Book 20061st editionics include tethered cord, vaginal reconstruction, continent catherizable channels, and the impact on family studies by? parents‘ organizations. The book not only carries on from the three previous editions by Douglas Stephens and Durham Smith (1963, 1971, and 1988) but assembles many new aspects in

敘述

https://doi.org/10.1007/978-3-658-01318-9current understanding of normal development and pathologic variations of ARM is incomplete, the critical period of organogenesis is understood to be at or before the 6–7. week of gestation. As a result, any aetiological defect would have to occur very early on in development.

轉(zhuǎn)向

Genetics, Pathogenesis and Epidemiology of Anorectal Malformations and Caudal Regression Syndromecurrent understanding of normal development and pathologic variations of ARM is incomplete, the critical period of organogenesis is understood to be at or before the 6–7. week of gestation. As a result, any aetiological defect would have to occur very early on in development.

蘑菇

https://doi.org/10.1007/978-3-540-31751-7Anorectal atresia; Anorectal malformations; Imperforate anus; Stool incontinence; Surgery; Surgical treat