000 01543 a2200457 4500
005 20250517215931.0
264 0 _c20190520
008 201905s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.38828
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRehder, Helga
245 0 0 _aPiepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibit.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_c07 2018
300 _a1559-1568 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aDwarfism
_xgenetics
650 0 4 _aExhibitions as Topic
650 0 4 _aFacies
650 0 4 _aFemale
650 0 4 _aFetal Diseases
_xgenetics
650 0 4 _aFilamins
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aOsteochondrodysplasias
_xgenetics
650 0 4 _aPrognosis
700 1 _aLaccone, Franco
700 1 _aKircher, Susanne G
700 1 _aSchild, Ralf L
700 1 _aRapp, Christiane
700 1 _aBald, Rainer
700 1 _aSchulze, Bernt
700 1 _aBehunova, Jana
700 1 _aNeesen, Juergen
700 1 _aSchoner, Katharina
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 176
_gno. 7
_gp. 1559-1568
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.38828
_zAvailable from publisher's website
999 _c28426598
_d28426598