000 01514 a2200505 4500
005 20250511212639.0
264 0 _c19911030
008 199110s 0 0 eng d
022 _a0340-6717
024 7 _a10.1007/BF00209018
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPierquin, G
245 0 0 _aTwo unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome.
_h[electronic resource]
260 _bHuman genetics
_cSep 1991
300 _a587-91 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aChromosome Banding
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 1
650 0 4 _aChromosomes, Human, Pair 6
650 0 4 _aCollagen
_xmetabolism
650 0 4 _aFace
_xabnormalities
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aJoint Dislocations
_xdiagnosis
650 0 4 _aKaryotyping
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aSkin
_xmetabolism
650 0 4 _aSyndrome
650 0 4 _aTrisomy
700 1 _aVan Regemorter, N
700 1 _aFourneau, C
700 1 _aBormans, J
700 1 _aFoerster, M
700 1 _aDamis, E
700 1 _aCremer-Perlmutter, N
700 1 _aLapiere, C M
700 1 _aVamos, E
773 0 _tHuman genetics
_gvol. 87
_gno. 5
_gp. 587-91
856 4 0 _uhttps://doi.org/10.1007/BF00209018
_zAvailable from publisher's website
999 _c1922960
_d1922960