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Quoted phrase not found in phrase index: "Neurodevelopmental disorder with microcephaly, hypotonia, and absent language"
Page 1
Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion.
J Med Genet. 1996 Feb;33(2):107-12. doi: 10.1136/jmg.33.2.107.
J Med Genet. 1996.
PMID: 8929945
Free PMC article.
Review.
Short stature was not invariable, 5/26 (19%) were on or above the 50th centile. Hypotonia at birth was recorded in 15/24 (63%) and neonatal feeding difficulties were recorded in 20/26 (77%). ...In our group of deletional cases, 100% showed severe mental retardation, ataxic …
Short stature was not invariable, 5/26 (19%) were on or above the 50th centile. Hypotonia at birth was recorded in 15/24 (63%) and ne …
Global developmental delay in a 10-month-old infant boy.
Blum NJ, Bird LM, Stein MT.
Blum NJ, et al.
J Dev Behav Pediatr. 2009 Feb;30(1):72-4. doi: 10.1097/DBP.0b013e3181976a83.
J Dev Behav Pediatr. 2009.
PMID: 19218848
On physical examination, the pediatrician found an alert, smiling child, but she was surprised by the following observations: unable to sit without support, absent pincer grasp, no audible language, unilateral exotropia, and microcephaly. ...She concluded tha …
On physical examination, the pediatrician found an alert, smiling child, but she was surprised by the following observations: unable to sit …
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