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Journal Article
JOURNAL OF HUMAN GENETICS, ISSN 1434-5161, 09/2019, Volume 64, Issue 9, pp. 885 - 890
Pediatric hypertension can cause hypertensive emergencies, including hemorrhagic stroke, contributing to rare but serious childhood morbidity and mortality.... 
FIBROMUSCULAR DYSPLASIA | DISEASE | GENETICS & HEREDITY | CHILDREN
Journal Article
Clinics, ISSN 1807-5932, 2018, Volume 73, p. e324
OBJECTIVES: To characterize the natural history of 39 achondroplastic patients diagnosed by clinical, radiological and molecular assessments. METHODS:... 
Achondroplasia | Growth | FGFR3 | Natural history | MEDICINE, GENERAL & INTERNAL | Natural History | MUTATIONS | CHILDREN | Original
Journal Article
International Journal of Agriculture and Biology, ISSN 1560-8530, 2014, Volume 16, Issue 6, pp. 1177 - 1182
Light-emitting diodes have been tested as alternative light sources in plant growth facilities. It was discovered that growth of green perilla is specifically... 
Light-emitting diode (LED) | Fresh vegetable | Artificial light source | Differential growth response | Wavelength interval | Plant growth facility | PLANT | LETTUCE | RED-LIGHT | LEAVES | COORDINATION | LEDS | ANTHOCYANIN | BIOSYNTHESIS | AGRICULTURE, MULTIDISCIPLINARY | LEAF | PHOTOSYNTHESIS | Production management | Usage | Analysis | Jalapeno | Hot peppers | Research | Light-emitting diodes | Growth (Plants)
Journal Article
Revista CEFAC, ISSN 1516-1846, 2019, Volume 21, Issue 5
ABSTRACT Purpose: to describe the audiological characteristics of patients with mucopolysaccharidosis. Methods: after formulating the research question, three... 
Journal Article
2001, Chʻopʻan., Pang Ir-yŏng Munhwa Chaedan Hanʼguk munhwa yesul chʻongsŏ, ISBN 8932310750, Volume 6, 439
Book
Estudos de Psicologia (Campinas), ISSN 0103-166X, 2019, Volume 36
Abstract The 22q11.2 Deletion Syndrome (22q11.2DS), the most common human chromosome microdeletion syndrome, is associated with a very heterogeneous... 
Journal Article
2008, Yŏngsang sanŏp chŏngch'aek yŏn'gu, ISBN 8980210639, Volume 7-6, 167
Book
American Journal of Human Genetics, ISSN 0002-9297, 03/2012, Volume 90, Issue 3, p. 494
Multicentric carpotarsal osteolysis (MCTO) is a rare skeletal dysplasia characterized by aggressive osteolysis, particularly affecting the carpal and tarsal... 
Genetics | Mutation | Bone diseases
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, p. 308
Floating-Harbor syndrome (FHS) is a rare condition characterized by short stature, delayed osseous maturation, expressive-language deficits, and a distinctive... 
Proteins | Genetic disorders | Genomics | Genetic research | Mutation | Binding sites
Journal Article
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