119 related articles for article (PubMed ID: 23918592)
1. Three patients resembling Teebi-Shaltout syndrome.
Aldemir O; Ozen S; Erdem S; Kiraz A; Akarsu N; Alanay Y
Am J Med Genet A; 2013 Oct; 161A(10):2570-5. PubMed ID: 23918592
[TBL] [Abstract][Full Text] [Related]
2. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
Froster UG; Rehder H; Höhn W; Oberheuser F
Am J Med Genet; 1993 Oct; 47(5):717-22. PubMed ID: 8267003
[TBL] [Abstract][Full Text] [Related]
3. Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndrome.
Bhoj EJ; Li D; Harr MH; Tian L; Wang T; Zhao Y; Qiu H; Kim C; Hoffman JD; Hakonarson H; Zackai EH
Am J Med Genet A; 2015 Nov; 167A(11):2497-502. PubMed ID: 26111080
[TBL] [Abstract][Full Text] [Related]
4. A new autosomal recessive disorder resembling Weaver syndrome.
Teebi AS; Sundareshan TS; Hammouri MY; al-Awadi SA; al-Saleh QA
Am J Med Genet; 1989 Aug; 33(4):479-82. PubMed ID: 2596508
[TBL] [Abstract][Full Text] [Related]
5. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage.
Teebi AS; Shaltout AA
Am J Med Genet; 1989 May; 33(1):58-60. PubMed ID: 2750786
[No Abstract] [Full Text] [Related]
6. Occipital atretic cephalocele, striking facial anomalies, and large feet in three siblings of a consanguineous union.
Zechi-Ceide RM; Guion-Almeida ML; Zanchetta S; Richieri-Costa A
Am J Med Genet A; 2007 Dec; 143A(24):3295-301. PubMed ID: 17907157
[TBL] [Abstract][Full Text] [Related]
7. A case report on autosomal recessive Robinow syndrome.
Eronat N; Cogulu D; Ozkinay F
Eur J Paediatr Dent; 2009 Sep; 10(3):147-50. PubMed ID: 19761290
[TBL] [Abstract][Full Text] [Related]
8. Prominent and elongated coccyx, a new manifestation of KBG syndrome associated with novel mutation in ANKRD11.
De Bernardi ML; Ivanovski I; Caraffi SG; Maini I; Street ME; Bayat A; Zollino M; Lepri FR; Gnazzo M; Errichiello E; Superti-Furga A; Garavelli L
Am J Med Genet A; 2018 Sep; 176(9):1991-1995. PubMed ID: 30088855
[TBL] [Abstract][Full Text] [Related]
9. Autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance.
al-Gazali LI; Bakalinova D
Clin Dysmorphol; 1998 Jul; 7(3):177-84. PubMed ID: 9689990
[TBL] [Abstract][Full Text] [Related]
10. Cardio-facio-cutaneous (CFC) syndrome--a distinct entity? Report of three patients demonstrating the diagnostic difficulties in delineation of CFC syndrome.
Wieczorek D; Majewski F; Gillessen-Kaesbach G
Clin Genet; 1997 Jul; 52(1):37-46. PubMed ID: 9272711
[TBL] [Abstract][Full Text] [Related]
11. Teebi hypertelorism syndrome: additional cases.
Machado-Paula LA; Guion-Almeida ML
Am J Med Genet A; 2003 Mar; 117A(2):181-3. PubMed ID: 12567419
[TBL] [Abstract][Full Text] [Related]
12. Microcephaly, dysmorphic features, corneal dystrophy, hairy nipples, underdeveloped labioscrotal folds, and small cerebellum in four patients.
Kayserili H; Altunoglu U; Yesil G; Rosti RÖ
Am J Med Genet A; 2016 Jun; 170(6):1391-9. PubMed ID: 27075597
[TBL] [Abstract][Full Text] [Related]
13. Finlay-Marks syndrome: report of two siblings and review of literature.
Naik P; Kini P; Chopra D; Gupta Y
Am J Med Genet A; 2012 Jul; 158A(7):1696-701. PubMed ID: 22639454
[TBL] [Abstract][Full Text] [Related]
14. Pai syndrome: report of seven South American patients.
Guion-Almeida ML; Mellado C; Beltrán C; Richieri-Costa A
Am J Med Genet A; 2007 Dec; 143A(24):3273-9. PubMed ID: 17907143
[TBL] [Abstract][Full Text] [Related]
15. Absent lacrimal ducts, distichiasis, dysmorphic features, and brachydactyly: a case report.
Holder-Espinasse M; de Blois MC; Faivre L; Romana S; Uteza Y; Munnich A; Lyonnet S; Cormier-Daire V; Amiel J
Clin Dysmorphol; 2001 Oct; 10(4):253-5. PubMed ID: 11665998
[TBL] [Abstract][Full Text] [Related]
16. Teebi hypertelorism syndrome: further observations.
Tsukahara M; Uchida M; Shinohara T
Am J Med Genet; 1995 Oct; 59(1):59-61. PubMed ID: 8849013
[TBL] [Abstract][Full Text] [Related]
17. Cutaneous findings in a new syndrome of autosomal recessive ectodermal dysplasia with corkscrew hairs.
Abramovits-Ackerman W; Bustos T; Simosa-Leon V; Fernandez L; Ramella M
J Am Acad Dermatol; 1992 Dec; 27(6 Pt 1):917-21. PubMed ID: 1479096
[TBL] [Abstract][Full Text] [Related]
18. Hay-Wells syndrome (AEC): a case report.
Macias E; de Carlos F; Cobo J
Oral Dis; 2006 Sep; 12(5):506-8. PubMed ID: 16910923
[TBL] [Abstract][Full Text] [Related]
19. Slow growth of hair and nails, craniofacial abnormalities and brachyphalangy.
Gruber R; Schossig AS; Alnutaifi KA; Martinz V; Blunder S; Zschocke J; Schmuth M; Tinschert S
J Dtsch Dermatol Ges; 2013 Oct; 11(10):1023-5. PubMed ID: 23668231
[No Abstract] [Full Text] [Related]
20. [A case of Kabuki syndrome admitted for acute diarrhea and growth retardation in a French hospital in tropical area].
Santiago J; Muszlak M; Goulois E; Ranaivoarivony V; Hébert JC; Lacombe D; Verloes A
Arch Pediatr; 2010 May; 17(5):588-93. PubMed ID: 20138485
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]