282 related articles for article (PubMed ID: 6721654)
1. [Congenital familial dwarfism with cephaloskeletal dysplasia (Taybi-Linder syndrome)].
Lavollay B; Faure C; Filipe G; Branca G; Huet de Barochez Y
Arch Fr Pediatr; 1984 Jan; 41(1):57-60. PubMed ID: 6721654
[TBL] [Abstract][Full Text] [Related]
2. Congenital familial dwarfism with cephalo-skeletal dysplasia.
Thomas PS; Nevin NC
Ann Radiol (Paris); 1976; 19(1):187-92. PubMed ID: 984702
[No Abstract] [Full Text] [Related]
3. Cephaloskeletal dysplasia (Taybi-Linder syndrome: osteodysplastic primordial dwarfism type III): report of two cases and review of the literature.
Vichi GF; Currarino G; Wasserman RL; Duvina PL; Filippi L
Pediatr Radiol; 2000 Sep; 30(9):644-52. PubMed ID: 11009306
[TBL] [Abstract][Full Text] [Related]
4. [Sublethal microcephalic chondrodysplasia. Taybi-Linder syndrome, primordial microcephalic nanism types I and III].
Maroteaux P; Badoual J
Arch Fr Pediatr; 1990 Feb; 47(2):103-6. PubMed ID: 2327863
[TBL] [Abstract][Full Text] [Related]
5. Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literature.
Sigaudy S; Toutain A; Moncla A; Fredouille C; Bourlière B; Ayme S; Philip N
Am J Med Genet; 1998 Oct; 80(1):16-24. PubMed ID: 9800907
[TBL] [Abstract][Full Text] [Related]
6. Familial congenital micromelic dysplasia with dislocation of radius and distinct face: a new skeletal dysplasia syndrome.
Borochowitz Z; Barak M; Hershkowitz S
Am J Med Genet; 1991 Apr; 39(1):91-6. PubMed ID: 1867270
[TBL] [Abstract][Full Text] [Related]
7. [Familial pelvi-scapulary dysplasia with anomalies of the epiphyses, dwarfism and dysmorphy: a new syndrome? (author's transl)].
Cousin J; Walbaum R; Cegarra P; Huguet J; Louis J; Pauli A; Fournier A; Fontaine G
Arch Fr Pediatr; 1982 Mar; 39(3):173-5. PubMed ID: 7103674
[TBL] [Abstract][Full Text] [Related]
8. A new skeletal dysplasia syndrome with dwarfism, craniofacial anomalies, and unique radiographic findings.
Jones KL; Jones KL; Miller K
Am J Med Genet; 1986 Mar; 23(3):751-7. PubMed ID: 2420178
[TBL] [Abstract][Full Text] [Related]
9. Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
Chemke J; Carmi R; Galil A; Bar-Ziv Y; Ben-Ytzhak I; Zurkowski L
Am J Med Genet; 1992 Aug; 43(6):989-95. PubMed ID: 1415350
[TBL] [Abstract][Full Text] [Related]
10. Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of the literature.
Klinge L; Schaper J; Wieczorek D; Voit T
Neuropediatrics; 2002 Dec; 33(6):309-13. PubMed ID: 12571786
[TBL] [Abstract][Full Text] [Related]
11. [Camptomelic dysplasia. A case of survival for more than 4 years].
Noyal P; Vermeulin G; Hibon D; Meck JM
Arch Fr Pediatr; 1982 Oct; 39(8):621-4. PubMed ID: 7159163
[TBL] [Abstract][Full Text] [Related]
12. Short rib-polydactyly syndrome, Majewski type.
Chen H; Yang SS; Gonzalez E; Fowler M; Al Saadi A
Am J Med Genet; 1980; 7(2):215-22. PubMed ID: 7468649
[TBL] [Abstract][Full Text] [Related]
13. Microcephalic osteodysplastic primordial dwarfism and cephalo-skeletal dysplasia (Taybi-Linder syndrome).
Taybi H
Am J Med Genet; 1992 Jun; 43(3):628-9. PubMed ID: 1605263
[No Abstract] [Full Text] [Related]
14. Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome.
Putoux A; Alqahtani A; Pinson L; Paulussen AD; Michel J; Besson A; Mazoyer S; Borg I; Nampoothiri S; Vasiljevic A; Uwineza A; Boggio D; Champion F; de Die-Smulders CE; Gardeitchik T; van Putten WK; Perez MJ; Musizzano Y; Razavi F; Drunat S; Verloes A; Hennekam R; Guibaud L; Alix E; Sanlaville D; Lesca G; Edery P
Clin Genet; 2016 Dec; 90(6):550-555. PubMed ID: 27040866
[TBL] [Abstract][Full Text] [Related]
15. New autosomal recessive syndrome of mental retardation, epilepsy, short stature, and skeletal dysplasia.
Gurrieri F; Sammito V; Bellussi A; Neri G
Am J Med Genet; 1992 Oct; 44(3):315-20. PubMed ID: 1488978
[No Abstract] [Full Text] [Related]
16. Microcephalic, osteodysplastic, primordial dwarfism.
Kozlowski K; Donovan T; Masel J; Wright RG
Australas Radiol; 1993 Feb; 37(1):111-4. PubMed ID: 8323498
[TBL] [Abstract][Full Text] [Related]
17. The SPONASTRIME dysplasia: familial short-limb dwarfism with saddle nose, spinal alterations and metaphyseal striation. Report of 4 siblings.
Fanconi S; Issler C; Giedion A; Prader A
Helv Paediatr Acta; 1983 Aug; 38(3):267-80. PubMed ID: 6618893
[TBL] [Abstract][Full Text] [Related]
18. Management of maxillofacial deformities in a patient with campomelic dysplasia.
Mintz SM; Adibfar A
J Oral Maxillofac Surg; 1994 Jun; 52(6):618-23. PubMed ID: 8189301
[No Abstract] [Full Text] [Related]
19. Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology.
Borochowitz Z; Langer LO; Gruber HE; Lachman R; Katznelson MB; Rimoin DL
Am J Med Genet; 1993 Feb; 45(3):320-6. PubMed ID: 8434618
[TBL] [Abstract][Full Text] [Related]
20. The neurologic findings in Taybi-Linder syndrome (MOPD I/III): case report and review of the literature.
Pierce MJ; Morse RP
Am J Med Genet A; 2012 Mar; 158A(3):606-10. PubMed ID: 22302400
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]