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Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndrome.
J Pediatr Endocrinol Metab. 2012;25(9-10):991-5. doi: 10.1515/jpem-2012-0103.
J Pediatr Endocrinol Metab. 2012.
PMID: 23426831
Cryptic del/dup aberration of 60.6 Mb at 5q15-5q23.3 predicting adult-onset leukodystrophy.
Jaklin C, Heiliger K, Hempel M, Sollacher D, Cohen M, Makowski CC, Meitinger T, Jauch A, Oexle K.
Jaklin C, et al. Among authors: heiliger k.
Eur J Med Genet. 2012 Oct;55(10):568-72. doi: 10.1016/j.ejmg.2012.06.010. Epub 2012 Jul 7.
Eur J Med Genet. 2012.
PMID: 22776853
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Anal atresia, coloboma, microphthalmia, and nasal skin tag in a female patient with 3.5 Mb deletion of 3q26 encompassing SOX2.
Salem NJ, Hempel M, Heiliger KJ, Hosie S, Meitinger T, Oexle K.
Salem NJ, et al. Among authors: heiliger kj.
Am J Med Genet A. 2013 Jun;161A(6):1421-4. doi: 10.1002/ajmg.a.35883. Epub 2013 Apr 23.
Am J Med Genet A. 2013.
PMID: 23613260
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Novel candidate genes of thyroid tumourigenesis identified in Trk-T1 transgenic mice.
Heiliger KJ, Hess J, Vitagliano D, Salerno P, Braselmann H, Salvatore G, Ugolini C, Summerer I, Bogdanova T, Unger K, Thomas G, Santoro M, Zitzelsberger H.
Heiliger KJ, et al.
Endocr Relat Cancer. 2012 May 24;19(3):409-21. doi: 10.1530/ERC-11-0387. Print 2012 Jun.
Endocr Relat Cancer. 2012.
PMID: 22454401
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Mycoplasma contamination of murine embryonic stem cells affects cell parameters, germline transmission and chimeric progeny.
Markoullis K, Bulian D, Hölzlwimmer G, Quintanilla-Martinez L, Heiliger KJ, Zitzelsberger H, Scherb H, Mysliwietz J, Uphoff CC, Drexler HG, Adler T, Busch DH, Schmidt J, Mahabir E.
Markoullis K, et al. Among authors: heiliger kj.
Transgenic Res. 2009 Feb;18(1):71-87. doi: 10.1007/s11248-008-9218-z. Epub 2008 Sep 26.
Transgenic Res. 2009.
PMID: 18819014
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