158 related articles for article (PubMed ID: 2729357)
21. [Disease picture of congenital bowing of long bones].
Rupprecht E; Manitz U
Helv Paediatr Acta; 1973 Nov; 28(5):467-76. PubMed ID: 4773227
[No Abstract] [Full Text] [Related]
22. Presentation of six cases of Stüve-Wiedemann syndrome.
Cormier-Daire V; Munnich A; Lyonnet S; Rustin P; Delezoide AL; Maroteaux P; Le Merrer M
Pediatr Radiol; 1998 Oct; 28(10):776-80. PubMed ID: 9799300
[TBL] [Abstract][Full Text] [Related]
23. Long-term observation of a patient with dominant omodysplasia.
Gordon BL; Champaigne NL; Rogers RC; Frias JL; Leroy JG
Am J Med Genet A; 2014 May; 164A(5):1234-8. PubMed ID: 24458798
[TBL] [Abstract][Full Text] [Related]
24. [Bilateral femoral hypoplasia in an adult male (author's transl)].
Leone G
Radiol Med; 1981 Mar; 67(3):141-6. PubMed ID: 7268085
[TBL] [Abstract][Full Text] [Related]
25. Fibrochondrogenesis in a 17-week fetus: a case expanding the phenotype.
Hunt NC; Vujanić GM
Am J Med Genet; 1998 Jan; 75(3):326-9. PubMed ID: 9475607
[TBL] [Abstract][Full Text] [Related]
26. Congenital bowing of the long bones. An example of a campomelic syndrome of the short-limbed normocephalic subtype.
Fryns JP; Annicq P; Ulrix M; van den Berghe H
Acta Paediatr Scand; 1983 Sep; 72(5):789-91. PubMed ID: 6637478
[TBL] [Abstract][Full Text] [Related]
27. Congenital distal humeral dysplasia: a case report.
Joseph B; Varghese RA
Pediatr Radiol; 2003 Jan; 33(1):7-10. PubMed ID: 12497228
[TBL] [Abstract][Full Text] [Related]
28. A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia.
Saal HM; Prows CA; Guerreiro I; Donlin M; Knudson L; Sund KL; Chang CF; Brugmann SA; Stottmann RW
Hum Mol Genet; 2015 Jun; 24(12):3399-409. PubMed ID: 25759469
[TBL] [Abstract][Full Text] [Related]
29. A new dwarfing syndrome with extreme shortening of humeri and severe coxa vara.
Patterson C; Lowry RB
Radiology; 1975 Feb; 114(2):341-2. PubMed ID: 1111001
[TBL] [Abstract][Full Text] [Related]
30. Isolated congenital bowed long bones.
Kapur S; Van Vloten A
Clin Genet; 1986 Feb; 29(2):165-7. PubMed ID: 3955869
[TBL] [Abstract][Full Text] [Related]
31. Unusual facies, arthrogryposis, advanced skeletal maturation and unique bone changes. A new congenital malformation syndrome.
Jequier S; Kozlowski K
Pediatr Radiol; 1987; 17(5):405-8. PubMed ID: 3627861
[TBL] [Abstract][Full Text] [Related]
32. A new lethal chondrodysplasia with platyspondyly, long bone angulation and mixed bone density.
Seller MJ; Berry AC; Maxwell D; McLennan A; Hall CM
Clin Dysmorphol; 1996 Jul; 5(3):213-5. PubMed ID: 8818449
[TBL] [Abstract][Full Text] [Related]
33. Familial rhizomelic dysplasia: phenotypic variation or heterogeneity?
Viljoen D; Goldblatt J; Wallis C; Beighton P
Am J Med Genet; 1987 Apr; 26(4):941-7. PubMed ID: 3591839
[TBL] [Abstract][Full Text] [Related]
34. Further delineation of Raine syndrome.
Al-Gazali LI; Jehier K; Nazih B; Abtin F; Haas D; Sadagahatian R
Clin Dysmorphol; 2003 Apr; 12(2):89-93. PubMed ID: 12868469
[TBL] [Abstract][Full Text] [Related]
35. Autosomal recessive omodysplasia: early prenatal diagnosis and a possible clue to the gene location.
Tan TY; McGillivray G; Kornman L; Fink AM; Superti-Furga A; Bonafé L; Francis DI; Savarirayan R
Am J Med Genet A; 2005 Jun; 135(3):324-7. PubMed ID: 15887278
[TBL] [Abstract][Full Text] [Related]
36. Additional malformations in femoral hypoplasia: unusual facies syndrome.
Verma A; Jain N; Jain K
Indian J Pediatr; 2002 Jun; 69(6):531-2. PubMed ID: 12139143
[TBL] [Abstract][Full Text] [Related]
37. Opsismodysplasia: a new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebrae.
Maroteaux P; Stanescu V; Stanescu R; Le Marec B; Moraine C; Lejarraga H
Am J Med Genet; 1984 Sep; 19(1):171-82. PubMed ID: 6496568
[TBL] [Abstract][Full Text] [Related]
38. A new familial short stature syndrome: Brussels type.
Mievis C; Claus D; Clapuyt P; Nyssen-Behets C; Gosseye S; Malvaux P; Verellen-Dumoulin C
Clin Dysmorphol; 1996 Jan; 5(1):9-16. PubMed ID: 8867654
[TBL] [Abstract][Full Text] [Related]
39. A dominantly inherited spondylometaphyseal dysplasia with "corner fractures" and congenital scoliosis.
Sutton VR; Hyland JC; Phillips WA; Schlesinger AE; Brill PW
Am J Med Genet A; 2005 Mar; 133A(2):209-12. PubMed ID: 15666313
[TBL] [Abstract][Full Text] [Related]
40. [Femoral hypoplasia and unusual facies. A syndrome of variable expressivity].
Selman E; Cantín A; Bancalari A
Rev Chil Pediatr; 1984; 55(2):100-3. PubMed ID: 6473848
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]