133 related articles for article (PubMed ID: 12687665)
1. Two familial cases with a lethal gracile bone dysplasia and intrauterine growth retardation.
Korniszewski L; Arbuckle S; Kozlowski K
Am J Med Genet A; 2003 May; 118A(4):343-9. PubMed ID: 12687665
[TBL] [Abstract][Full Text] [Related]
2. Fibrochondrogenesis: radiologic and histologic studies.
Eteson DJ; Adomian GE; Ornoy A; Koide T; Sugiura Y; Calabro A; Lungarotti S; Mastroiacovo P; Lachman RS; Rimoin DL
Am J Med Genet; 1984 Oct; 19(2):277-90. PubMed ID: 6507479
[TBL] [Abstract][Full Text] [Related]
3. Schneckenbecken dysplasia in fetus: report of four cases.
Lahmar-Boufaroua A; Yacoubi MT; Belaid L; Delezoide AL
Fetal Diagn Ther; 2009; 25(2):216-9. PubMed ID: 19407457
[TBL] [Abstract][Full Text] [Related]
4. A distinct lethal neonatal chondrodysplasia with snail-like pelvis: Schneckenbecken dysplasia.
Borochowitz Z; Jones KL; Silbey R; Adomian G; Lachman R; Rimoin DL
Am J Med Genet; 1986 Sep; 25(1):47-59. PubMed ID: 3799723
[TBL] [Abstract][Full Text] [Related]
5. Radiological evolution in IMAGe association: a case report.
Amano N; Naoaki H; Ishii T; Narumi S; Hachiya R; Nishimura G; Hasegawa T
Am J Med Genet A; 2008 Aug; 146A(16):2130-3. PubMed ID: 18627061
[TBL] [Abstract][Full Text] [Related]
6. Thin ribs, thin tubular bones, abnormal facies and intrauterine growth retardation: a lethal syndrome.
Sharma BK; Kapoor R; Ramji S; Thirupuram S; Suri M
Br J Radiol; 1990 Aug; 63(752):654-6. PubMed ID: 2400886
[No Abstract] [Full Text] [Related]
7. Metatropic dysplasia lethal variants.
Hall CM; Elçioglu NH
Pediatr Radiol; 2004 Jan; 34(1):66-74. PubMed ID: 14566438
[TBL] [Abstract][Full Text] [Related]
8. Ultrasonographic prenatal diagnosis of microcephalic osteodysplastic primordial dwarfism types I/III.
Nadjari M; Fasouliotis SJ; Ariel I; Raas-Rothschild A; Bar-Ziv J; Elchalal U
Prenat Diagn; 2000 Aug; 20(8):666-9. PubMed ID: 10951479
[TBL] [Abstract][Full Text] [Related]
9. Oto-palato-digital syndrome, type II: report of three cases with further delineation of the chondro-osseous morphology.
Savarirayan R; Cormier-Daire V; Unger S; Lachman RS; Roughley PJ; Wagner SF; Rimoin DL; Wilcox WR
Am J Med Genet; 2000 Nov; 95(3):193-200. PubMed ID: 11102922
[TBL] [Abstract][Full Text] [Related]
10. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL).
Tsirikos AI; Mason DE; Scott CI; Chang WN
Am J Med Genet A; 2003 Jun; 119A(3):386-90. PubMed ID: 12784311
[TBL] [Abstract][Full Text] [Related]
11. A female case of Sedaghatian type spondylometaphyseal dysplasia.
Foulds N; Fairhurst J; Temple IK; Cade S; Groves C; Lancaster T
Am J Med Genet A; 2003 May; 118A(4):377-81. PubMed ID: 12687672
[TBL] [Abstract][Full Text] [Related]
12. Giant-cell chondrodysplasia in a male infant with clinical and radiological findings resembling the Piepkorn type of lethal osteochondrodysplasia.
Urioste M; Rodríguez JI; Bofarull JM; Torán N; Ferrer C; Villa A
Am J Med Genet; 1997 Jan; 68(3):342-6. PubMed ID: 9024569
[TBL] [Abstract][Full Text] [Related]
13. Extra pelvic ossification centers in thanatophoric dysplasia and platyspondylic lethal skeletal dysplasia-San Diego type.
Kitoh H; Lachman RS; Brodie SG; Mekikian PB; Rimoin DL; Wilcox WR
Pediatr Radiol; 1998 Oct; 28(10):759-63. PubMed ID: 9799297
[TBL] [Abstract][Full Text] [Related]
14. Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic or Hall type: report of a case with normal face and literature review.
Sulko J; Kozlowski K
J Pediatr Orthop B; 2008 Nov; 17(6):323-7. PubMed ID: 18841068
[TBL] [Abstract][Full Text] [Related]
15. Schimke immuno-osseous dysplasia: two cases.
Tylki-Szymańska A; Pyrkosz A; Krajewska-Walasek M; Michałkiewicz J; Kowalska A; Rokicki D
Pediatr Radiol; 2003 Mar; 33(3):216-8. PubMed ID: 12612825
[TBL] [Abstract][Full Text] [Related]
16. [The chondrodystrophic child].
Tenhaeff D; Büttinghaus K; Moayer M; Callies R
Geburtshilfe Frauenheilkd; 1972 Aug; 32(8):666-70. PubMed ID: 4561127
[No Abstract] [Full Text] [Related]
17. [Familial osteochondrodysplatic dwarfism associated with deafness and tapeto-retinal heredo-degeneration].
Khaldi F; Bennaceur B; Gharbi HA
Arch Fr Pediatr; 1989; 46(6):429-32. PubMed ID: 2783003
[TBL] [Abstract][Full Text] [Related]
18. Gracile bone dysplasia.
Thomas JA; Rimoin DL; Lachman RS; Wilcox WR
Am J Med Genet; 1998 Jan; 75(1):95-100. PubMed ID: 9450865
[TBL] [Abstract][Full Text] [Related]
19. Spondylometaphyseal dysplasia Sedaghatian type associated with lethal arrhythmia and normal intrauterine growth in three siblings.
Kerr B; Smith V; Patel R; Ladusans E; Sillence DO
Clin Dysmorphol; 2000 Jul; 9(3):167-72. PubMed ID: 10955475
[TBL] [Abstract][Full Text] [Related]
20. Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathology.
Whitley CB; Langer LO; Ophoven J; Gilbert EF; Gonzalez CH; Mammel M; Coleman M; Rosemberg S; Rodriques CJ; Sibley R
Am J Med Genet; 1984 Oct; 19(2):265-75. PubMed ID: 6507478
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
