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Meta Gene, ISSN 2214-5400, 02/2017, Volume 11, pp. 147 - 151
We report a familial case of Simpson-Golabi-Behmel syndrome type 1 (SGBS1) with prenatal ultrasound findings of bilateral ventriculomegaly and polyhydramnios... 
GPC4-TFDP3 intergenic deletion | Simpson-Golabi-Behmel syndrome type 1 (SGBS1) | GPC3 intragenic deletion
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 09/2012, Volume 158A, Issue 9, pp. 2245 - 2249
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 04/2019, Volume 62, Issue 4, pp. 243 - 247
and are the only two genes in which mutations are known to cause Simpson-Golabi-Behmel syndrome type 1 (SGBS1). The majority of SGBS1 patients have point... 
Intellectual disability | Congenital anomalies | GPC3 | Overgrowth | GPC4 | X-linked disorder | Simpson-golabi-behmel syndrome | XQ26 | GENETICS & HEREDITY | PATIENT | MUTATIONS | CLUSTER | GLYPICAN GENE | PRENATAL-DIAGNOSIS | Hernia | Genetic disorders | Gene mutations | Children's hospitals | Genes | Medical genetics | Genetic research | Family | Congenital heart disease | Index Medicus
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 03/2014, Volume 164, Issue 3, pp. 774 - 777
Journal Article
Journal Article
Journal Article
Journal Article
Journal of Stomatology, Oral and Maxillofacial Surgery, ISSN 2468-7855, 2018
Simpson-Golabi-Behmel Syndrome (SGBS) is an X-linked overgrowth syndrome characterized by pre- and post-natal overgrowth, typical facial appearance and... 
Jaw lesions | Simpson-Golabi-Behmel syndrome | Ameloblastoma | Synchronous | Odontogenic keratocyst
Journal Article
Taiwanese Journal of Obstetrics and Gynecology, ISSN 1028-4559, 2012, Volume 51, Issue 2, pp. 186 - 191
Abstract With the advent of prenatal sonography, fetal overgrowth can be easily detected. Prenatal-onset overgrowth can be secondary to normal variants of... 
Internal Medicine | Obstetrics and Gynecology | Simpson-Golabi-Behmel syndrome | Beckwith-Wiedemann syndrome | Sotos syndrome | overgrowth | fetus | Fetus | Overgrowth | MUTATION ANALYSIS | I SYNDROME | INCREASED NUCHAL TRANSLUCENCY | NSD1 GENE | PHENOTYPE | FOLLOW-UP | ASSISTED REPRODUCTIVE TECHNOLOGIES | IDENTIFICATION | OBSTETRICS & GYNECOLOGY | GPC3 | GLYPICAN GENE
Journal Article
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, ISSN 1552-4868, 05/2013, Volume 163, Issue 2, pp. 92 - 105
Journal Article
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