150 related articles for article (PubMed ID: 8297075)
1. Corneal changes in chondrodysplasia punctata syndrome.
Spierer A; Neumann D
Ann Ophthalmol; 1993 Sep; 25(9):356-8. PubMed ID: 8297075
[TBL] [Abstract][Full Text] [Related]
2. [Congenital epiphyseal chondrodysplasia punctata. Study of 9 cases].
Frontera Izquierdo P; Cabezuelo Huerta G; Malo Concepción P
An Esp Pediatr; 1985 Sep; 23(3):175-82. PubMed ID: 4073686
[TBL] [Abstract][Full Text] [Related]
3. [Ocular findings in reno-facial dysplasia (Potter-syndrome) (author's transl)].
Daicker B; Gysin P
Klin Monbl Augenheilkd; 1978 Sep; 173(3):334-41. PubMed ID: 108456
[TBL] [Abstract][Full Text] [Related]
4. Chondrodysplasia punctata with multiple congenital anomalies: a new syndrome?
Mortier GR; Messiaen LM; Espeel M; Smets KJ; Vanzieleghem BD; Roels F; De Paepe AM
Pediatr Radiol; 1998 Oct; 28(10):790-3. PubMed ID: 9799302
[TBL] [Abstract][Full Text] [Related]
5. Microspherophakia in association with the rhizomelic form of chondrodysplasia punctata.
Eustis HS; Yaplee SM; Kogutt M; Ginsberg HG
J Pediatr Ophthalmol Strabismus; 1990; 27(5):237-41. PubMed ID: 2246735
[TBL] [Abstract][Full Text] [Related]
6. [Alcohol embryopathy with symptomatic chondrodysplasia punctata. The 4th published case].
Paditz E; Rupprecht E
Helv Paediatr Acta; 1985 Apr; 40(1):61-8. PubMed ID: 3855176
[TBL] [Abstract][Full Text] [Related]
7. Provisionally unique autosomal recessive chondrodysplasia punctata syndrome.
Toriello HV; Higgins JV; Miller T
Am J Med Genet; 1993 Oct; 47(5):797-9. PubMed ID: 8267015
[TBL] [Abstract][Full Text] [Related]
8. Chondrodysplasia punctata, tibia-metacarpal (MT) type.
Rittler M; Menger H; Spranger J
Am J Med Genet; 1990 Oct; 37(2):200-8. PubMed ID: 2248286
[TBL] [Abstract][Full Text] [Related]
9. [Congenital cataract in genetically determined syndromes].
Böke W; Hilgenberg F
Med Monatsschr; 1967 Mar; 21(3):110-3. PubMed ID: 4875204
[No Abstract] [Full Text] [Related]
10. [Congenital and infantile cataract].
Nordmann J
Ber Zusammenkunft Dtsch Ophthalmol Ges; 1969; 69():283-91. PubMed ID: 5395058
[No Abstract] [Full Text] [Related]
11. Chondrodysplasia punctata in a nine-year-old girl presenting as "unclassified multiple malformation syndrome".
Kozlowski K
Pediatr Radiol; 1980 Jul; 9(4):236-8. PubMed ID: 7402749
[TBL] [Abstract][Full Text] [Related]
12. A case of bilateral dysplasia epiphysealis hemimelica associated with polydactyly and syndactyly.
Takegami Y; Nogami H
Clin Orthop Relat Res; 1993 Nov; (296):307-9. PubMed ID: 8222443
[TBL] [Abstract][Full Text] [Related]
13. [Conradi-H:unermann chondrodysplasia punctata and fetal alcoholism].
Sarda P; Guillaumont S; Jalaguier J; Bonnet H
J Genet Hum; 1989 Dec; 37(4-5):395-9. PubMed ID: 2635716
[TBL] [Abstract][Full Text] [Related]
14. [Glaucoma in Conradi's syndrome].
Damel A; Manzitti E
Arch Oftalmol B Aires; 1966; 41(1):4-6. PubMed ID: 5914630
[No Abstract] [Full Text] [Related]
15. X-linked dominant chondrodysplasia punctata/ichthyosis/cataract syndrome in males.
Happle R
Am J Med Genet; 1995 Jul; 57(3):493. PubMed ID: 7677158
[No Abstract] [Full Text] [Related]
16. Conradi-Hünermann-Happle syndrome (X-linked dominant chondrodysplasia punctata) confirmed by plasma sterol and mutation analysis.
Kolb-Mäurer A; Grzeschik KH; Haas D; Bröcker EB; Hamm H
Acta Derm Venereol; 2008; 88(1):47-51. PubMed ID: 18176751
[TBL] [Abstract][Full Text] [Related]
17. Osebold-Remondini syndrome vs chondrodysplasia punctata.
Sheffield LJ; Mayne VM; Danks DM
Am J Med Genet; 1987 Oct; 28(2):507, 509. PubMed ID: 3425625
[No Abstract] [Full Text] [Related]
18. [Laryngeal atresia in an infant with chondrodysplasia punctata, rhizomelic type].
Storm W; Fasse M
Monatsschr Kinderheilkd; 1991 Sep; 139(9):629-31. PubMed ID: 1745255
[TBL] [Abstract][Full Text] [Related]
19. [Congenital chondroangiopathia punctata (major type). Clinical, radiographic and anatomo-histologic study in a premature infant].
Centa A; Doria-Miglietta F
Pathologica; 1967; 59(877):359-66. PubMed ID: 5620183
[No Abstract] [Full Text] [Related]
20. Serum lipid analysis confirms the diagnosis of X-linked dominant chondrodysplasia punctata - Conradi-Hünermann-Happle syndrome.
Lindenthal B; Repgen R; Emons D; Lentze MJ; von Bergmann K; Lütjohann D
Klin Padiatr; 2004; 216(2):67-9. PubMed ID: 15106076
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
