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Indian Journal of Human Genetics, ISSN 0971-6866, 2014, Volume 20, Issue 1, pp. 72 - 74
Raine syndrome is a rare genetic disorder with characteristic features of exophthalmos, choanal atresia or stenosis, osteosclerosis and cerebral... 
Lethal | osteosclerosis | Raine syndrome | Case studies | Care and treatment | Dysplasia | Patient outcomes | Bone diseases | Diagnosis | Risk factors | Case Report
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 2016, Volume 59, Issue 11, pp. 577 - 583
Abstract Raine syndrome is a rare autosomal recessive bone dysplasia characterized by characteristic facial features with exophthalmos and generalized... 
Medical Education | Raine syndrome | FAM20C gene | Kohlschutter-Tonz syndrome | OSTEOSCLEROTIC BONE DYSPLASIA | DENTINOGENESIS | GENETICS & HEREDITY | FAM20C | MUTATIONS | AMELOGENESIS | Cleft Palate - diagnosis | Microcephaly - genetics | Seizures - genetics | Bone Diseases, Developmental - mortality | Casein Kinase I - genetics | Humans | Dementia - diagnosis | Dementia - physiopathology | Learning Disorders - physiopathology | Male | Cleft Palate - genetics | Epilepsy - mortality | Microcephaly - mortality | Abnormalities, Multiple - mortality | Amelogenesis Imperfecta - genetics | Bone Diseases, Developmental - genetics | Epilepsy - physiopathology | Exophthalmos - mortality | Dementia - genetics | Bone Diseases, Developmental - physiopathology | Osteosclerosis - mortality | Seizures - physiopathology | Amelogenesis Imperfecta - diagnosis | Exophthalmos - genetics | Amelogenesis Imperfecta - mortality | Epilepsy - genetics | Female | Microcephaly - physiopathology | Osteosclerosis - genetics | Abnormalities, Multiple - genetics | Diagnosis, Differential | Cleft Palate - mortality | Osteosclerosis - diagnosis | Amelogenesis Imperfecta - physiopathology | Extracellular Matrix Proteins - genetics | Microcephaly - diagnosis | Exophthalmos - physiopathology | Cleft Palate - physiopathology | Abnormalities, Multiple - physiopathology | Exophthalmos - diagnosis | Dementia - mortality | Epilepsy - diagnosis | Phenotype | Abnormalities, Multiple - diagnosis | Adolescent | Learning Disorders - genetics | Osteosclerosis - physiopathology | Biodegradation | Dysplasia | Learning disabilities | Diagnosis | Seizures (Medicine) | Casein | Index Medicus
Journal Article
Fertility and Sterility, ISSN 0015-0282, 2011, Volume 95, Issue 7, pp. 2347 - 2353.e1
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 12/2015, Volume 16, Issue 1, pp. 8 - 8
Journal Article
Journal of Gastroenterology and Hepatology, ISSN 0815-9319, 05/2016, Volume 31, Issue 5, pp. 980 - 987
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 09/2019, Volume 179, Issue 9, pp. 1866 - 1871
Journal Article
Human Reproduction, ISSN 0268-1161, 03/2019, Volume 34, Issue 3, pp. 389 - 402
Abstract STUDY QUESTION Are early signs of metabolic disorder in late adolescence associated with features of impaired testicular function many years before... 
Raine | semen | testicular volume | reproductive hormones | testicular function | metabolic | MORTALITY | CARDIOMETABOLIC RISK | OBSTETRICS & GYNECOLOGY | IMPACT | REPRODUCTIVE BIOLOGY | INSULIN-RESISTANCE | MEN | FATTY LIVER | INFERTILITY | BODY-MASS INDEX | VALUES | ADIPOSITY
Journal Article
Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2009, Volume 48, Issue 8, pp. 800 - 809
Journal Article
PLoS Genetics, ISSN 1553-7390, 05/2016, Volume 12, Issue 5, pp. e1006037 - e1006037
Journal Article
Dicle Medical Journal / Dicle Tıp Dergisi, ISSN 1300-2945, 01/2014, Volume 41, Issue 2, pp. 401 - 404
Ultrasonography technical developments in the early diagnosis of fetal anomalies in utero has helped. However, a very rare anomaly in utero, or diagnosed late... 
prenatal diagnosis | Raine syndrome
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 12/2013, Volume 161, Issue 12, pp. 3155 - 3160
Journal Article