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1929, Spisy Filosofické fakulty Masarykovy university v Brně, čís. 29, 255
Book
American Journal of Surgical Pathology, ISSN 0147-5185, 2016, Volume 40, Issue 7, pp. 876 - 885
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 03/2016, Volume 170, Issue 3, pp. 559 - 564
Costello syndrome (CS) entails a cancer predisposition and is caused by activating HRAS mutations, typically arising de novo in the paternal germline.... 
mutation | imprinting | p.Q22K | Beckwith–Wiedemann syndrome | Costello syndrome | neonatal hyperinsulinemic hypoglycemia | 11p15.5 | loss of heterozygosity | HRAS | Beckwith-Wiedemann syndrome | HRAS mutation | Neonatal hyperinsulinemic hypoglycemia | Imprinting | Loss of heterozygosity | P.Q22K | DEFECTS | ABNORMALITIES | GENOTYPE | HRAS(G12V) | HRAS MUTATION ANALYSIS | ORIGIN | PHENOTYPE CORRELATION | GENETICS & HEREDITY | GERMLINE MUTATIONS | RHABDOMYOSARCOMA | PATHWAY SYNDROME | Uniparental Disomy - diagnosis | Genomic Imprinting | Proto-Oncogene Proteins p21(ras) - genetics | Costello Syndrome - diagnosis | Humans | Beckwith-Wiedemann Syndrome - diagnosis | Molecular Sequence Data | Infant | Male | Hypoglycemia - pathology | Loss of Heterozygosity | Beckwith-Wiedemann Syndrome - genetics | Inheritance Patterns | Congenital Hyperinsulinism - genetics | Congenital Hyperinsulinism - pathology | Insulin-Like Growth Factor II - genetics | Base Sequence | Fatal Outcome | Clone Cells | Hypoglycemia - diagnosis | Hypoglycemia - genetics | Costello Syndrome - pathology | Congenital Hyperinsulinism - diagnosis | Chromosomes, Human, Pair 11 - chemistry | Pancreas - pathology | Pancreas - metabolism | Costello Syndrome - genetics | Uniparental Disomy - genetics | Beckwith-Wiedemann Syndrome - pathology | Uniparental Disomy - pathology | Amino Acid Substitution | Infants (Newborn) | Immunohistochemistry | Index Medicus
Journal Article
British Journal of Dermatology, ISSN 0007-0963, 11/2018, Volume 179, Issue 5, pp. 1031 - 1032
Linked Article : Prieto‐Barrios et al. Br J Dermatol 2018; 179 :1163–1167 . 
PHAKOMATOSIS PIGMENTOKERATOTICA | POSTZYGOTIC HRAS MUTATION | DERMATOLOGY | Carcinogenesis | Index Medicus
Journal Article
Reliability Engineering and System Safety, ISSN 0951-8320, 2018
The fundamental issue in reference to human reliability analysis (HRA) in a nuclear power plant is the lack of empirical data for human error probability (HEP)... 
Simulator data | Human error probability | HRA data | Human performance data | Human reliability analysis (HRA)
Journal Article
American journal of medical genetics. Part A, ISSN 1552-4825, 9/2015, Volume 167A, Issue 9, pp. 2085 - 2097
Heterozygous germline mutations in the proto-oncogene HRAS cause Costello syndrome (CS), an intellectual disability condition with severe failure-to-thrive,... 
HRAS p.Gly60Asp | rasopathy | HRAS germline mutation | RAS-pathway disorder | Noonan syndrome | Costello syndrome
Journal Article
Pathology, research and practice, 08/2019, pp. 152549 - 152549
Journal Article
Cancer Research, ISSN 0008-5472, 05/2012, Volume 72, Issue 10, pp. 2457 - 2467
Journal Article
02/2008
Costello syndrome is a rare, distinctive, multiple congenital anomaly syndrome, characterized by soft, loose skin with deep palmar and plantar creases, loose... 
Costello syndrome | papillomas | Dysmorphic facies | Acanthosis nigricans | HRAS
Web Resource
International Journal of Dermatology, ISSN 0011-9059, 01/2018, Volume 57, Issue 1, pp. 120 - 122
Journal Article
International Journal of Cancer, ISSN 0020-7136, 2016, Volume 138, Issue 9, p. 2201
One out of ten patients with pheochromocytoma (PCC) and paraganglioma (PGL) develop malignant disease. Today there are no reliable pathological methods to... 
Surgery | neuroendocrine tumor | HRAS | Kirurgi | massively parallel sequencing
Journal Article
1996, ISBN 9788090141667
Book
Journal Article