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Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 10/2018, Volume 52, Issue S1, pp. 71 - 71
Journal Article
Case Report - Poland syndrome (anomaly) with congenital hemangioma: A new association, 12/2006
Unilateral defect of pectoral muscle and ipsilateral syndactyly constitute Poland syndrome. Absence or hypoplasia of the breast and nipple, axillary hair loss... 
Congenital hemangioma, Poland syndrome, Polydactyly
Journal
Journal Article
Clinical Genetics, ISSN 0009-9163, 04/2019, Volume 95, Issue 4, pp. 540 - 541
Journal Article
12/2011
McKusick-Kaufman syndrome (MKS, OMIM #236700) is a rare syndrome inherited in an autosomal recessive pattern with a phenotypic triad comprising... 
McKusick-Kaufman syndrome | polydactyly | Hydrometrocolpos
Web Resource
Korean Journal of Dermatology, ISSN 0494-4739, 03/2018, Volume 56, Issue 3, pp. 202 - 205
Journal Article
대한피부과학회지, ISSN 0494-4739, 2018, Volume 56, Issue 3, p. 202
Rudimentary polydactyly is a congenital anomaly of the hand clinically ranging from a small wart-like tumor to a pedunculated structure near the thumb or... 
Rudimentary polydactyly
Journal Article
Congenital Anomalies, ISSN 0914-3505, 09/2016, Volume 56, Issue 5, pp. 226 - 232
Journal Article
The Journal of Bone and Joint Surgery, ISSN 0021-9355, 08/2016, Volume 98, Issue 15, pp. 1298 - 1306
BACKGROUND:Polydactyly at the medial side of the foot (“medial polydactyly” of the foot) is a rare and diverse congenital anomaly. In order to plan and... 
SURGERY | TOE | ORTHOPEDICS | THUMB | Radiography | Foot - surgery | Reproducibility of Results | Humans | Female | Infant | Male | Polydactyly - diagnosis | Polydactyly - surgery | Polydactyly - classification | Polydactyly - diagnostic imaging | Foot - diagnostic imaging | Index Medicus | Abridged Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 01/2011, Volume 88, Issue 1, pp. 106 - 114
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 04/2012, Volume 21, Issue 8, pp. 1808 - 1823
Journal Article
Journal Article
Clinical Endocrinology, ISSN 0300-0664, 09/2018, Volume 89, Issue 3, pp. 378 - 380
Congenital panhypopituitarism refers to the deficiency of two or more pituitary hormones in the newborn. It is a rare condition of which early recognition is... 
HYPOPITUITARISM | ENDOCRINOLOGY & METABOLISM | Polydactyly
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2011, Volume 88, Issue 4, pp. 508 - 515
Journal Article
Journal of Hand Surgery, ISSN 0363-5023, 2014, Volume 39, Issue 8, pp. 1549 - 1552
Purpose To report long-term outcomes (> 10 y) after radial polydactyly reconstruction. Methods We evaluated 43 surgically reconstructed thumbs in 41 patients... 
Orthopedics | radial polydactyly split thumbs | thumb polydactyly | thumb duplication | Preaxial polydactyly | SURGERY | ORTHOPEDICS | SURGICAL-TREATMENT | Young Adult | Reoperation | Humans | Adolescent | Thumb - surgery | Adult | Female | Male | Polydactyly - surgery | Child | Reconstructive Surgical Procedures | Children's hospitals | Index Medicus
Journal Article
Journal of Hand Surgery, ISSN 0363-5023, 09/2017, Volume 42, Issue 9, pp. 753.e1 - 753.e6
To introduce the “on-top plasty” technique and report our long-term outcomes. We evaluated 5 thumbs in 5 patients who underwent radial polydactyly... 
on-top plasty | thumb polydactyly | thumb duplication | Radial polydactyly
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 11/2011, Volume 89, Issue 5, pp. 634 - 643
Journal Article
2008, Volume 2, 1
Reference
Clinical Genetics, ISSN 0009-9163, 08/2019, Volume 96, Issue 2, pp. 134 - 139
Pre‐axial polydactyly (PPD) is characterized by well‐developed non‐functional 1st digit (thumb) duplication in hands and/or feet. It is mostly inherited in... 
limb anomaly | nonsense variant | STKLD1 | pre‐axial polydactyly | serine‐threonine kinase | REGULATOR | SPLICE-SITE VARIANT | SHH | pre-axial polydactyly | KINASE | GENETICS & HEREDITY | NEK1 | serine-threonine kinase | Amino acids | Family | Genetic aspects | Mutation | Nonsense mutation | Chromosome 9 | Polydactyly
Journal Article