143 related articles for article (PubMed ID: 8985729)
1. Oculocerebrocutaneous syndrome: a case report, a follow-up, and differential diagnostic considerations.
Moog U; Krüger G; Stengel B; De Die-Smulders C; Dykstra S; Bleeker-Wagemakers E
Genet Couns; 1996; 7(4):257-65. PubMed ID: 8985729
[TBL] [Abstract][Full Text] [Related]
2. Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype.
Moog U; Jones MC; Bird LM; Dobyns WB
J Med Genet; 2005 Dec; 42(12):913-21. PubMed ID: 15879499
[TBL] [Abstract][Full Text] [Related]
3. Delleman syndrome: report of a case with a mild phenotype.
Cambiaghi S; Levet PS; Guala G; Baldini D; Gianotti R
Eur J Dermatol; 2000 Dec; 10(8):623-6. PubMed ID: 11125327
[TBL] [Abstract][Full Text] [Related]
4. Severe oculocerebrocutaneous (Delleman) syndrome: overlap with Goldenhar anomaly.
McCandless SE; Robin NH
Am J Med Genet; 1998 Jul; 78(3):282-5. PubMed ID: 9677067
[TBL] [Abstract][Full Text] [Related]
5. Ocular manifestations in Delleman syndrome (Oculocerebrocutaneous syndrome, OCC-syndrome) and encephalocraniocutaneous lipomatosis (ECCL). Report of three cases.
Narbay G; Meire F; Verloes A; Casteels I; Devos E
Bull Soc Belge Ophtalmol; 1996; 261():65-70. PubMed ID: 9009364
[TBL] [Abstract][Full Text] [Related]
6. Focal dermal hypoplasia with unusual cutaneous features.
Maymí MA; Martín-García RF
Pediatr Dermatol; 2007; 24(4):387-90. PubMed ID: 17845162
[TBL] [Abstract][Full Text] [Related]
7. [Focal dermal hypoplasia (Goltz syndrome) in the neonate: report of a case presenting with cleft lip and palate].
Nagalo K; Laberge JM; Nguyen VH; Laberge-Caouette L; Turgeon J
Arch Pediatr; 2012 Feb; 19(2):160-2. PubMed ID: 22178259
[TBL] [Abstract][Full Text] [Related]
8. Anophthalmia, intracerebral cysts, and cleft lip/palate: expansion of the phenotype in oculocerebrocutaneous syndrome?
Angle B; Hersh JH
Am J Med Genet; 1997 Jan; 68(1):39-42. PubMed ID: 8986273
[TBL] [Abstract][Full Text] [Related]
9. Delleman Oorthuys syndrome.
Rizvi SW; Siddiqui MA; Khan AA; Siddiqui Z
Middle East Afr J Ophthalmol; 2015; 22(1):122-4. PubMed ID: 25624688
[TBL] [Abstract][Full Text] [Related]
10. [Goltz syndrome with facial clefts. Etiopathogenetic considerations. Apropos of a new case].
Delaire J; David A; Stalder JF
Ann Pediatr (Paris); 1985 Dec; 32(10):847-54. PubMed ID: 3841471
[No Abstract] [Full Text] [Related]
11. Fryns anophthalmia-plus syndrome with hypoplastic adrenal glands.
Ozalp O; Ozcimen EE; Yilmaz Z; Yanik F; Sahin FI
Genet Couns; 2008; 19(1):43-6. PubMed ID: 18564500
[TBL] [Abstract][Full Text] [Related]
12. Oculocerebrocutaneous syndrome: report of three additional cases and aetiological considerations.
Moog U; de Die-Smulders C; Systermans JM; Cobben JM
Clin Genet; 1997 Oct; 52(4):219-25. PubMed ID: 9383027
[TBL] [Abstract][Full Text] [Related]
13. Anophthalmia, cleft lip/palate, facial anomalies, and CNS anomalies and hypothalamic disorder in a newborn: a midline developmental field defect.
Leichtman LG; Wood B; Rohn R
Am J Med Genet; 1994 Mar; 50(1):39-41. PubMed ID: 8160751
[TBL] [Abstract][Full Text] [Related]
14. Congenital accessory palpebral aperture--an addition to the spectrum of Delleman syndrome.
Manudhane A; Arora R; Kapoor S; Rastogi A; Goyal JL
Ophthalmic Genet; 2013; 34(1-2):109-11. PubMed ID: 23215914
[TBL] [Abstract][Full Text] [Related]
15. Fryns anophthalmia-plus syndrome in an 18-week-old fetus.
Jayasinghe C; Gembruch U; Kuchelmeister K; Körber F; Müller AM
Pediatr Dev Pathol; 2012; 15(1):58-61. PubMed ID: 21675878
[TBL] [Abstract][Full Text] [Related]
16. Oculocerebrocutaneous (Delleman) syndrome: report of two cases.
Pascual-Castroviejo I; Pascual-Pascual SI; Velázquez-Fragua R; Lapunzina P
Neuropediatrics; 2005 Feb; 36(1):50-4. PubMed ID: 15776323
[TBL] [Abstract][Full Text] [Related]
17. Neonatal palatal cysts and their morphology in cleft lip and palate.
Richard BM; Qiu CX; Ferguson MW
Br J Plast Surg; 2000 Oct; 53(7):555-8. PubMed ID: 11000069
[TBL] [Abstract][Full Text] [Related]
18. MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome.
Happle R; Daniëls O; Koopman RJ
Am J Med Genet; 1993 Oct; 47(5):710-3. PubMed ID: 8267001
[TBL] [Abstract][Full Text] [Related]
19. [Congenital serous cyst of the orbit with anophthalmos].
Ndiaye PA; Ndiaye MR; Sakho Y; Mendes V; Gueye M; Wade A
J Fr Ophtalmol; 1991; 14(3):195-8. PubMed ID: 1918826
[TBL] [Abstract][Full Text] [Related]
20. Hemifacial microsomia in a newborn with hypoplastic skin lesions, an eyelid skin tag, and microphthalmia: an unusual presentation of Delleman syndrome.
Ming JE; Katowitz J; McDonald-McGinn DM; Schnur RE; Hunter JV; Zackai EH
Clin Dysmorphol; 1998 Oct; 7(4):279-83. PubMed ID: 9823495
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
