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peters plus syndrome (16) 16
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02/2014
Background: Peters Plus syndrome (MIM 261540) is a rare autosomal recessive condition characterized by ocular defects (typically Peters anomaly) and other... 
Human | Peters-Plus Syndrome | Facial Dysmorphism with Multiple Malformations | B3GALTL Protein | Ambiguous Genitalia
Web Resource
The American Journal of Human Genetics, ISSN 0002-9297, 08/2019, Volume 105, Issue 2, pp. 425 - 433
While genetic causes are known for many syndromes involving developmental anomalies, a large number of individuals with overlapping phenotypes remain... 
WDR37 | dominant | syndrome | CRISPR-Cas9 | Peters plus | Walker-Warburg | seizures | zebrafish | coloboma | Peters | B3GALTL | MICROPHTHALMIA | MUTATIONS | PETERS PLUS SYNDROME | ANOPHTHALMIA | GENETICS & HEREDITY | Gene mutations | Physiological aspects | Child development deviations | Genetic aspects | Research | Risk factors | Developmental disabilities | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2017, Volume 12, Issue 9, pp. e0184903 - e0184903
Journal Article
Turkish journal of obstetrics and gynecology, ISSN 2149-9322, 12/2018, Volume 15, Issue 4, pp. 273 - 276
Peters plus syndrome is a rare congenital disorder that includes ocular anterior segment defects of the classic Peter's anomaly, and is mostly associated with... 
Cataracts | Medical personnel | Ultrasonic imaging | Nuclear magnetic resonance--NMR | Congenital diseases | Fetuses | Genes | Mutation | Chromosomes | Peters anomaly | Peters plus syndrome | congenital cataract | prenatal diagnosis | Case Report | B3GALTL gene
Journal Article
Iranian Journal of Pediatrics, ISSN 2008-2142, 2013, Volume 23, Issue 4, pp. 485 - 488
Background: Peters Plus syndrome (MIM 261540) is a rare autosomal recessive condition characterized by ocular defects (typically Peters anomaly) and other... 
Human | Facial dysmorphism with multiple malformations | Peters-plus syndrome | Ambiguous genitalia | B3GALTL protein | Peters-Plus Syndrome | B3GALTL Protein | PEDIATRICS | Facial Dysmorphism with Multiple Malformations | Ambiguous Genitalia | Case Report
Journal Article
Journal Article
Iranian Journal of Pediatrics, ISSN 1018-4406, 02/2014, Volume 23, Issue 4
Background: Peters Plus syndrome (MIM 261540) is a rare autosomal recessive condition characterized by ocular defects (typically Peters anomaly) and other... 
Human | Peters-Plus Syndrome | Facial Dysmorphism with Multiple Malformations | B3GALTL Protein | Ambiguous Genitalia
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 06/2013, Volume 161, Issue 6, pp. 1207 - 1213
Journal Article
Journal Article
01/2015, ISBN 9783709118825
GWAS | CRKL | SALL1 | GJA5 | Noonan syndrome | SALL4 | PITX2 | SOX7 | Edwards syndrome | PRKAB2 | NKX2-6 | Sotos syndrome | VSD | WNT5A | Adams–Oliver syndrome | Okihiro syndrome | MID1 | Opitz syndrome | CHARGE syndrome | MAML3 | ROR2 | NOTCH2 | NOTCH1 | GATA6 | CNV | GATA4 | Williams–Beuren syndrome | Frank–ter Haar syndrome | ASD | DVL1 | Atrial septal defect | Mowat–Wilson syndrome | Larsen-like syndrome | NKX2-5 | Ventricular septum | Char syndrome | MLL2 | Noncompaction | TFAP2B | Potocki–Lupski syndrome | JAG1 | Down syndrome | GDF3 | B3GALTL | BCL9 | Nodal | MKRN2 | NF1 | Peters plus syndrome | FGFR3 | TDGF1 | FBN1 | Townes–Brock syndrome | CITED2 | Holt–Oram syndrome | CHD7 | Ulnar–mammary syndrome | Robinow syndrome | CHD1 | Marfan syndrome | Diaphragmatic hernia | Trisomy 21 | NIPBL | Copy number variation | Cri-du-chat syndrome | Ellis–van Creveld syndrome | ZIC3 | ACP6 | SH3PXD2B | Kabuki syndrome | LVNC | Blepharophimosis syndrome | HRAS | LBR | EVC1 | Jacobsen syndrome | Patau syndrome | Ventricular septal defect | Kleefstra syndrome | Trisomy 18 | Velocardiofacial syndrome | Wolf–Hirschhorn syndrome | FOXL2 | Trisomy 13 | MYH7 | Muenke syndrome | DiGeorge syndrome | Alagille syndrome | CRYPTIC | Pallister–Killian syndrome | NSD1 | Pelger–Huet anomaly | TBX20 | GPC3 | HAS2 | Hypophosphatemia | SHOC2 | TNNI3 | EVC2 | Oculofaciocardiodental syndrome | TBX1 | Cornelia de Lange syndrome | Noonan-like syndrome | NTRK3 | IRX4 | PTPN11 | TBX5 | FMO5 | CFC1 | Ras/MAPK | TBX3 | 22q11 deletion syndrome | TBX15 | Costello syndrome | TGFβ | Simpson–Golabi–Behmel syndrome | BCOR | ZFHX1B
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