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Oncogene
|
August 16, 2006
Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas
R G Weber, A Hoischen, M Ehrler, et al.
Biorxiv : the Preprint Server for Biology
|
July 29, 2024
TRGT-denovo: accurate detection of <i>de novo</i> tandem repeat mutations
T Mokveld, E Dolzhenko, H Dashnow, et al.
Orphanet Journal of Rare Diseases
|
August 7, 2025
Genetic evaluation of five patients with ROHHAD-NET using whole genome sequencing and optical genome mapping
N van Engelen, H M van Santen, F van Dijk, et al.
Clinical Genetics
|
January 6, 2011
Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions
M H Willemsen, G Beunders, M Callaghan, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
May 8, 2021
The association between treatment and systemic inflammation in acromegaly
T L C Wolters, C D C C van der Heijden, O Pinzariu, et al.
Clinical Pharmacology and Therapeutics
|
May 10, 2017
Rare NOX3 Variants Confer Susceptibility to Agranulocytosis During Thyrostatic Treatment of Graves' Disease
T S Plantinga, P Arts, G H Knarren, et al.
Journal of Dental Research
|
August 3, 2017
Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing
A K Hoebel, D Drichel, M van de Vorst, et al.
Journal of Dental Research
|
November 12, 2016
Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing
K D Khandelwal, N Ishorst, H Zhou, et al.
Clinical Genetics
|
January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study
P Makrythanasis, B W van Bon, M Steehouwer, et al.
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of 2
Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Oncogene
|
August 16, 2006
Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas
R G Weber, A Hoischen, M Ehrler, et al.
Biorxiv : the Preprint Server for Biology
|
July 29, 2024
TRGT-denovo: accurate detection of <i>de novo</i> tandem repeat mutations
T Mokveld, E Dolzhenko, H Dashnow, et al.
Orphanet Journal of Rare Diseases
|
August 7, 2025
Genetic evaluation of five patients with ROHHAD-NET using whole genome sequencing and optical genome mapping
N van Engelen, H M van Santen, F van Dijk, et al.
Clinical Genetics
|
January 6, 2011
Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions
M H Willemsen, G Beunders, M Callaghan, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
May 8, 2021
The association between treatment and systemic inflammation in acromegaly
T L C Wolters, C D C C van der Heijden, O Pinzariu, et al.
Clinical Pharmacology and Therapeutics
|
May 10, 2017
Rare NOX3 Variants Confer Susceptibility to Agranulocytosis During Thyrostatic Treatment of Graves' Disease
T S Plantinga, P Arts, G H Knarren, et al.
Journal of Dental Research
|
August 3, 2017
Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing
A K Hoebel, D Drichel, M van de Vorst, et al.
Journal of Dental Research
|
November 12, 2016
Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing
K D Khandelwal, N Ishorst, H Zhou, et al.
Clinical Genetics
|
January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study
P Makrythanasis, B W van Bon, M Steehouwer, et al.
Page
of 2