143 related articles for article (PubMed ID: 15876767)
1. Fibrochondrogenesis.
Kulkarni ML; Matadh PS; Praveen Prabhu SP; Kulkarni PM
Indian J Pediatr; 2005 Apr; 72(4):355-7. PubMed ID: 15876767
[TBL] [Abstract][Full Text] [Related]
2. Fibrochondrogenesis.
Kulkarni ML; Matadh PS; Prabhu SP; Kulkarni PM
Indian J Pediatr; 2005 Apr; 72(4):355-357. PubMed ID: 28386830
[TBL] [Abstract][Full Text] [Related]
3. Two sibs with fibrochondrogenesis.
Leeners B; Funk A; Cotarelo CL; Sauer I
Am J Med Genet A; 2004 Jun; 127A(3):318-20. PubMed ID: 15150788
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Recurrence of fibrochondrogenesis in a consanguineous family.
al-Gazali LI; Bakir M; Dawodu A; Haas D
Clin Dysmorphol; 1999 Jan; 8(1):59-61. PubMed ID: 10327253
[TBL] [Abstract][Full Text] [Related]
6. A lethal skeletal dysplasia with generalised sclerosis and advanced skeletal maturation: Blomstrand chondrodysplasia?
Young ID; Zuccollo JM; Broderick NJ
J Med Genet; 1993 Feb; 30(2):155-7. PubMed ID: 8445622
[TBL] [Abstract][Full Text] [Related]
7. Birth prevalence and pattern of osteochondrodysplasias in an inbred high risk population.
Al-Gazali LI; Bakir M; Hamid Z; Varady E; Varghes M; Haas D; Bener A; Padmanabhan R; Abdulrrazzaq YM; Dawadu A
Birth Defects Res A Clin Mol Teratol; 2003 Feb; 67(2):125-32. PubMed ID: 12769508
[TBL] [Abstract][Full Text] [Related]
8. A new autosomal recessive lethal chondrodystrophy with congenital hydrops.
Greenberg CR; Rimoin DL; Gruber HE; DeSa DJ; Reed M; Lachman RS
Am J Med Genet; 1988 Mar; 29(3):623-32. PubMed ID: 3377005
[TBL] [Abstract][Full Text] [Related]
9. Autosomal recessive omodysplasia.
Stoll C; Pennerath A; Poirat P
Ann Genet; 1995; 38(2):97-101. PubMed ID: 7486832
[TBL] [Abstract][Full Text] [Related]
10. A family with spondyloepimetaphyseal dwarfism: a 'new' dysplasia or Kniest disease with autosomal recessive inheritance?
Farag TI; Al-Awadi SA; Hunt MC; Satyanath S; Zahran M; Usha R; Uma R
J Med Genet; 1987 Oct; 24(10):597-601. PubMed ID: 3681904
[TBL] [Abstract][Full Text] [Related]
11. Grebe chondrodysplasia and similar forms of severe short-limbed dwarfism.
Romeo G; Zonana J; Lachman RS; Opitz JM; Scott CI; Spranger JW; Rimoin DL
Birth Defects Orig Artic Ser; 1977; 13(3C):109-15. PubMed ID: 890106
[TBL] [Abstract][Full Text] [Related]
12. A new category of lethal short-limbed dwarfism.
Knowles S; Winter R; Rimoin D
Am J Med Genet; 1986 Sep; 25(1):41-6. PubMed ID: 3799722
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2.
Tompson SW; Faqeih EA; Ala-Kokko L; Hecht JT; Miki R; Funari T; Funari VA; Nevarez L; Krakow D; Cohn DH
Am J Med Genet A; 2012 Feb; 158A(2):309-14. PubMed ID: 22246659
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Spondyloepimetaphyseal dysplasia and abnormal dentition in siblings: a new autosomal recessive syndrome.
Rao V; Morton RE; Young ID
Clin Dysmorphol; 1997 Jan; 6(1):3-12. PubMed ID: 9018411
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of campomelic dysplasia by ultrasonography.
Winter R; Rosenkranz W; Hofmann H; Zierler H; Becker H; Borkenstein M
Prenat Diagn; 1985; 5(1):1-8. PubMed ID: 3883340
[TBL] [Abstract][Full Text] [Related]
18. Fibrochondrogenesis in male twins at 24 weeks gestation.
Bankier A; Fortune D; Duke J; Sillence DO
Am J Med Genet; 1991 Jan; 38(1):95-8. PubMed ID: 2012139
[TBL] [Abstract][Full Text] [Related]
19. [Mesomelic dwarfism. Pronounced form in a female infant of a father with dyschondrosteosis and a mother with Madelung's deformity].
Gugliantini P; Scapaticci A
Radiol Med; 1978 Apr; 64(4):433-44. PubMed ID: 704970
[TBL] [Abstract][Full Text] [Related]
20. Further evidence of POP1 mutations as the cause of anauxetic dysplasia.
Elalaoui SC; Laarabi FZ; Mansouri M; Mrani NA; Nishimura G; Sefiani A
Am J Med Genet A; 2016 Sep; 170(9):2462-5. PubMed ID: 27380734
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
