000 01491 a2200433 4500
005 20250513185834.0
264 0 _c19990824
008 199908s 0 0 eng d
022 _a0340-6199
024 7 _a10.1007/s004310051149
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aStumm, M
245 0 0 _aMosaic tetrasomy 9p in a girl with multiple congenital anomalies: cytogenetic and molecular-cytogenetic studies.
_h[electronic resource]
260 _bEuropean journal of pediatrics
_cJul 1999
300 _a571-5 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aAdolescent
650 0 4 _aBlindness
_xgenetics
650 0 4 _aBone and Bones
_xabnormalities
650 0 4 _aChromosome Aberrations
650 0 4 _aChromosome Disorders
650 0 4 _aChromosomes, Human, Pair 9
650 0 4 _aCraniofacial Abnormalities
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMosaicism
650 0 4 _aNucleic Acid Hybridization
650 0 4 _aSensitivity and Specificity
700 1 _aTönnies, H
700 1 _aMandon, U
700 1 _aGötze, A
700 1 _aKrebs, P
700 1 _aWieacker, P F
773 0 _tEuropean journal of pediatrics
_gvol. 158
_gno. 7
_gp. 571-5
856 4 0 _uhttps://doi.org/10.1007/s004310051149
_zAvailable from publisher's website
999 _c10370897
_d10370897