000 01315 a2200385 4500
005 20250517191218.0
264 0 _c20180903
008 201809s 0 0 eng d
022 _a1473-5717
024 7 _a10.1097/MCD.0000000000000207
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKlaphake, Sanne
245 0 0 _aA patient with chromosome 18p deletion and congenital hypoglossia.
_h[electronic resource]
260 _bClinical dysmorphology
_cApr 2018
300 _a46-48 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdolescent
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Disorders
_xgenetics
650 0 4 _aChromosomes, Human, Pair 18
_xgenetics
650 0 4 _aFemale
650 0 4 _aHoloprosencephaly
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aKaryotyping
650 0 4 _aStomatognathic System Abnormalities
_xgenetics
700 1 _avan Dooren, Marieke F
700 1 _aSenden, Richelle E M
700 1 _aHoogeboom, A Jeannette M
700 1 _aWolvius, Eppo B
700 1 _aKoudstaal, Maarten J
773 0 _tClinical dysmorphology
_gvol. 27
_gno. 2
_gp. 46-48
856 4 0 _uhttps://doi.org/10.1097/MCD.0000000000000207
_zAvailable from publisher's website
999 _c27875980
_d27875980