Jos Herbergs
Overview
Explore the profile of Jos Herbergs including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
98
Followers
0
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Recent Articles
1.
Dukers-Muijrers N, Wolffs P, Eppings L, Gotz H, Bruisten S, Schim van der Loeff M, et al.
BMC Infect Dis
. 2016 Aug;
16:381.
PMID: 27502928
Background: In women, anorectal infections with Chlamydia trachomatis (CT) are about as common as genital CT, yet the anorectal site remains largely untested in routine care. Anorectal CT frequently co-occurs...
2.
Weusten J, Herbergs J
Forensic Sci Int Genet
. 2011 Feb;
6(1):17-25.
PMID: 21295532
In forensic DNA profiling use is made of the well-known technique of PCR. When the amount of DNA is high, generally unambiguous profiles can be obtained, but for low copy...
3.
Paulussen A, Schrander-Stumpel C, Tserpelis D, Spee M, Stegmann A, Mancini G, et al.
Eur J Hum Genet
. 2010 Jun;
18(9):999-1005.
PMID: 20531442
Holoprosencephaly is a severe malformation of the brain characterized by abnormal formation and separation of the developing central nervous system. The prevalence is 1:250 during early embryogenesis, the live-born prevalence...
4.
Mosterd K, Sommer A, van Marion A, Lacko M, Herbergs J, de Bondt B, et al.
Dermatol Surg
. 2010 Jan;
35(12):2051-3.
PMID: 20050151
No abstract available.
5.
Stevens S, Smeets E, Blom E, van Uum C, Albrechts J, Herbergs J, et al.
Am J Med Genet A
. 2009 Sep;
149A(10):2226-30.
PMID: 19725130
Genotypic and phenotypic data are presented on three adult siblings with mild to moderate mental retardation and mild dysmorphic features. All three siblings showed a chromosome 20 gain at the...
6.
Roessler E, Lacbawan F, Dubourg C, Paulussen A, Herbergs J, Hehr U, et al.
Hum Mutat
. 2009 Jan;
30(4):E541-54.
PMID: 19177455
Mutations of the ZIC2 transcription factor gene are among the most common heterozygous variations detected in holoprosencephaly (HPE) patients, a patient group who lack critical midline forebrain specification due to...
7.
Koolen D, Herbergs J, Veltman J, Pfundt R, van Bokhoven H, Stroink H, et al.
J Hum Genet
. 2006 Jul;
51(8):721-726.
PMID: 16865294
Holoprosencephaly (HPE) is the most common developmental defect affecting the forebrain and midface in humans. The aetiology of HPE is highly heterogeneous and includes both environmental and genetic factors. Here...
8.
Moog U, Smeets E, van Roozendaal K, Schoenmakers S, Herbergs J, Schoonbrood-Lenssen A, et al.
Eur J Paediatr Neurol
. 2003 Mar;
7(1):5-12.
PMID: 12615169
Mutations in the MECP2 (methyl-CpG-binding protein 2) gene are known to cause Rett syndrome, a well-known and clinically defined neurodevelopmental disorder. Rett syndrome occurs almost exclusively in females and for...