000 01330 a2200361 4500
005 20250515224432.0
264 0 _c20100830
008 201008s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.33410
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aQidwai, Kanwal
245 0 0 _aDeletions of Xp provide evidence for the role of holocytochrome C-type synthase (HCCS) in congenital diaphragmatic hernia.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cJun 2010
300 _a1588-90 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural
650 0 4 _aChild
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, X
_xgenetics
650 0 4 _aHernia, Diaphragmatic
_xgenetics
650 0 4 _aHernias, Diaphragmatic, Congenital
650 0 4 _aHumans
650 0 4 _aLyases
_xgenetics
650 0 4 _aMale
700 1 _aPearson, David M
700 1 _aPatel, Gayle Simpson
700 1 _aPober, Barbara R
700 1 _aImmken, Ladonna L
700 1 _aCheung, Sau Wai
700 1 _aScott, Daryl A
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 152A
_gno. 6
_gp. 1588-90
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.33410
_zAvailable from publisher's website
999 _c19855901
_d19855901