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Journal Article
Best Practice & Research: Clinical Endocrinology & Metabolism, ISSN 1521-690X, 2010, Volume 25, Issue 1, pp. 161 - 179
Noonan syndrome is a relatively common, clinically variable developmental disorder. Cardinal features include postnatally reduced growth, distinctive facial... 
Endocrinology & Metabolism | pathogenetic mechanisms | Noonan syndrome | genotype-phenotype correlations | diagnosis | Noonan-like syndrome with loose anagen hair | LEOPARD syndrome | RAS signaling | patient management | CBL mutation-associated syndrome | LEOPARD-SYNDROME | SOMATIC PTPN11 MUTATIONS | GROWTH-HORMONE TREATMENT | OF-FUNCTION MUTATIONS | RAS SUPERFAMILY | PHENOTYPIC SPECTRUM | SHP2 MUTATIONS | ENDOCRINOLOGY & METABOLISM | JUVENILE MYELOMONOCYTIC LEUKEMIA | GERMLINE MUTATIONS | MYELODYSPLASTIC SYNDROMES | Loose Anagen Hair Syndrome - genetics | Costello Syndrome - diagnosis | Humans | LEOPARD Syndrome - genetics | Infant | Heart Defects, Congenital - genetics | Facies | SOS1 Protein - genetics | Failure to Thrive - diagnosis | Neurofibromatosis 1 - genetics | Child | Intracellular Signaling Peptides and Proteins - genetics | Noonan Syndrome - diagnosis | Proto-Oncogene Proteins c-cbl - genetics | Failure to Thrive - genetics | Proto-Oncogene Proteins c-raf - genetics | Ectodermal Dysplasia - diagnosis | Noonan Syndrome - genetics | Loose Anagen Hair Syndrome - diagnosis | Costello Syndrome - genetics | Proto-Oncogene Proteins B-raf - genetics | Adolescent | LEOPARD Syndrome - diagnosis | Heart Defects, Congenital - diagnosis | Mitogen-Activated Protein Kinases - genetics | Ectodermal Dysplasia - genetics | Protein Tyrosine Phosphatase, Non-Receptor Type 11 - genetics | Proteins | Developmental biology | Protein kinases
Journal Article
Human Mutation, ISSN 1059-7794, 2017, Volume 38, Issue 6, pp. 692 - 703
Journal Article
British Journal of Cancer, ISSN 0007-0920, 04/2015, Volume 112, Issue 8, pp. 1392 - 1397
Journal Article
Pediatrics, ISSN 0031-4005, 2014, Volume 134, Issue 4, pp. e1149 - e1162
Journal Article
Human Mutation, ISSN 1059-7794, 12/2017, Volume 38, Issue 12, pp. 1671 - 1683
Journal Article
Veterinary Record, ISSN 0042-4900, 06/2015, Volume 176, Issue 23, pp. 596 - 596
Genetic susceptibility or resistance to diseases is currently drawing increasing attention. This work describes two different breeding herds showing signs of... 
VETERINARY SCIENCES | Failure to Thrive - veterinary | Genetic Predisposition to Disease | Swine Diseases - genetics | Animals | Failure to Thrive - genetics | Swine | Weaning | Male
Journal Article
Veterinary Record, ISSN 0042-4900, 07/2018, Volume 183, Issue 3, p. 95
Porcine periweaning failure to thrive syndrome (PFTS) can be defined by anorexia, lethargy, progressive debilitation and compulsive behaviours that occur in... 
PFTS | GWAS | SNP | PIG | PIGS | INDIVIDUALS | VETERINARY SCIENCES | MICE | WIDE ASSOCIATION | FEATURES | Failure to Thrive - veterinary | Swine Diseases - genetics | Animals | Failure to Thrive - genetics | Swine | Weaning | Female | Genotype | Male | Polymorphism, Single Nucleotide | Case-Control Studies
Journal Article
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 2014, Volume 51, Issue 1, pp. 10 - 20
Journal Article