short stature phenotype

Related entities (4)

Mentioned in (35)

Papers in which this entity is mentioned.

• Specificity, length and luck drive gene rankings in association studies. (2026)
• Gastrulation-stage alcohol exposure induces similar rates of craniofacial malformations in male and female C57BL/6J mice. (2024)
• Characteristics of the Symptoms of the Proposed ND-PAE Disorder in First Grade Children in a Community Sample. (2024)
• A saturated map of common genetic variants associated with human height. (2022)
• Fetal alcohol spectrum disorder predisposes to metabolic abnormalities in adulthood. (2020)
• Clinical presentation, diagnosis, and management of fetal alcohol spectrum disorder. (2019)
• Comparison of the 4-Digit Code, Canadian 2015, Australian 2016 and Hoyme 2016 fetal alcohol spectrum disorder diagnostic guidelines. (2019)
• Heavy Prenatal Alcohol Exposure is Related to Smaller Corpus Callosum in Newborn MRI Scans. (2017)
• De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
• Transcriptome Profiling Identifies Ribosome Biogenesis as a Target of Alcohol Teratogenicity and Vulnerability during Early Embryogenesis. (2017)
• Altered Parietal Activation during Non-symbolic Number Comparison in Children with Prenatal Alcohol Exposure. (2017)
• Clinical Assessment and Diagnosis of Germline Predisposition to Hematopoietic Malignancies: The University of Chicago Experience. (2017)
• The Essential Role of Growth Deficiency in the Diagnosis of Fetal Alcohol Spectrum Disorder. (2016)
• Parietal dysfunction during number processing in children with fetal alcohol spectrum disorders. (2015)
• Maternal risk factors for fetal alcohol spectrum disorders in a province in Italy. (2014)
• Characterization of subtle brain abnormalities in a mouse model of Hedgehog pathway antagonist-induced cleft lip and palate. (2014)
• High-throughput transcriptome sequencing identifies candidate genetic modifiers of vulnerability to fetal alcohol spectrum disorders. (2014)
• Genomic factors that shape craniofacial outcome and neural crest vulnerability in FASD. (2014)
• Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly. (2013)
• Commonality in Down and fetal alcohol syndromes. (2013)
• Approaching the prevalence of the full spectrum of fetal alcohol spectrum disorders in a South African population-based study. (2013)
• Impaired delay and trace eyeblink conditioning in school-age children with fetal alcohol syndrome. (2011)
• Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants. (2011)
• Cleft lip and palate results from Hedgehog signaling antagonism in the mouse: Phenotypic characterization and clinical implications. (2010)
• Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome. (2010)
• A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion. (2010)
• On the value of homogeneous constructs for construct validation, theory testing, and the description of psychopathology. (2009)
• Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. (2009)
• Prenatal alcohol exposure and interhemispheric transfer of tactile information: Detroit and Cape Town findings. (2009)
• Facial Image Classification of Mouse Embryos for the Animal Model Study of Fetal Alcohol Syndrome. (2009)
• Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia. (2008)
• Fetal alcohol spectrum disorders and their persisting sequelae in adult life. (2008)
• Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughters. (2008)
• Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans. (2006)
• A Long-Term Perspective of FAS. (1994)

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