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ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 12/2019, Volume 14, Issue 1, pp. 281 - 10
Journal Article
Contemporary clinical dentistry, ISSN 0976-237X, 04/2012, Volume 3, Issue 2, pp. 205 - 208
The ectodermal dysplasias (EDs) are a large and complex group of diseases. More than 170 different clinical conditions have been recognized and defined as... 
Case studies | Care and treatment | Diagnosis | EEC syndrome | Hair | Transplants & implants | Intellectual disabilities | Mouth | Fingers & toes | Teeth | Skin | Hearing impairment | Defects | ectrodactyly | Case Report | Ectodermal dysplasia
Journal Article
Wiley Interdisciplinary Reviews: Developmental Biology, ISSN 1759-7684, 05/2015, Volume 4, Issue 3, pp. 215 - 266
Journal Article
Balkan Journal of Medical Genetics, ISSN 1311-0160, 01/2012, Volume 15, Issue 1, pp. 51 - 54
Hidrotic ectodermal dysplasia type 2 (HED2) or Clouston syndrome (OMIM #129500) is a rare autosomal dominant genetic disorder which affects skin and its... 
Hidrotic ectodermal dysplasia type 2 (HED2) | Cx30 | Clouston syndrome | GJB6 | HIDROTIC ECTODERMAL DYSPLASIA | GENE | GENETICS & HEREDITY | MUTATIONS | Case Report
Journal Article
Current Genomics, ISSN 1389-2029, 06/2015, Volume 16, Issue 4, pp. 264 - 278
Radial deficiencies (RDs), defined as under/abnormal development or absence of any of the structures of the forearm, radial carpal bones and thumb, occur with... 
Radial deficiency | Congenital upper limb anomalies | Thumb hypoplasia | VATER-ASSOCIATION | APICAL ECTODERMAL RIDGE | BIOCHEMISTRY & MOLECULAR BIOLOGY | TETHERED SPINAL-CORD | CONGENITAL-ANOMALIES | FANCONI-ANEMIA | UPPER-LIMB ANOMALIES | TOWNES-BROCKS-SYNDROME | GENETICS & HEREDITY | HOLT-ORAM-SYNDROME | RENAL-OCULAR SYNDROME | BALLER-GEROLD-SYNDROME
Journal Article