185 related articles for article (PubMed ID: 2801767)
1. Epiphyseal dysplasia with coxa vara, microcephaly, and normal intelligence in sibs: expanded spectrum of Lowry-Wood syndrome?
Hankenson LG; Ozonoff MB; Cassidy SB
Am J Med Genet; 1989 Jul; 33(3):336-40. PubMed ID: 2801767
[TBL] [Abstract][Full Text] [Related]
2. Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia--Lowry-Wood syndrome.
Nevin NC; Thomas PS; Hutchinson J
Am J Med Genet; 1986 May; 24(1):33-9. PubMed ID: 3706411
[TBL] [Abstract][Full Text] [Related]
3. Syndrome of epiphyseal dysplasia, short stature, microcephaly and nystagmus.
Lowry RB; Wood BJ
Clin Genet; 1975 Oct; 8(4):269-74. PubMed ID: 1183069
[TBL] [Abstract][Full Text] [Related]
4. Multiple joint dislocations: an additional skeletal finding in Lowry-Wood syndrome?
Magnani C; Tedesco SA; Dallaglio S; Sommi M; Bacchini E; Vetro A; Zuffardi O; Bevilacqua G
Am J Med Genet A; 2009 Feb; 149A(4):737-41. PubMed ID: 19288552
[TBL] [Abstract][Full Text] [Related]
5. Epiphyseal dysplasia, microcephaly, nystagmus, and retinitis pigmentosa.
Lowry RB; Wood BJ; Cox TA; Hayden MR
Am J Med Genet; 1989 Jul; 33(3):341-5. PubMed ID: 2801768
[TBL] [Abstract][Full Text] [Related]
6. Patterson-Lowry rhizomelic dysplasia: report of two new patients.
Franceschini P; Licata D; Guala A; Ingrosso G; Di Cara G; Franceschini D
Am J Med Genet A; 2004 May; 127A(1):86-92. PubMed ID: 15103724
[TBL] [Abstract][Full Text] [Related]
7. The expanding phenotype of RNU4ATAC pathogenic variants to Lowry Wood syndrome.
Farach LS; Little ME; Duker AL; Logan CV; Jackson A; Hecht JT; Bober M
Am J Med Genet A; 2018 Feb; 176(2):465-469. PubMed ID: 29265708
[TBL] [Abstract][Full Text] [Related]
8. Infantile coxa vara.
Pavlov H; Goldman AB; Freiberger RH
Radiology; 1980 Jun; 135(3):631-40. PubMed ID: 7384448
[TBL] [Abstract][Full Text] [Related]
9. Hip pathology in Majewski osteodysplastic primordial dwarfism type II.
Karatas AF; Bober MB; Rogers K; Duker AL; Ditro CP; Mackenzie WG
J Pediatr Orthop; 2014 Sep; 34(6):585-90. PubMed ID: 24705347
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Spondylometaphyseal dysplasia, corner fracture type: a heritable condition associated with coxa vara.
Langer LO; Brill PW; Ozonoff MB; Pauli RM; Wilson WG; Alford BA; Pavlov H; Drake DG
Radiology; 1990 Jun; 175(3):761-6. PubMed ID: 2343127
[TBL] [Abstract][Full Text] [Related]
12. Developmental coxa vara associated with spondylometaphyseal dysplasia (DCV/SMD): "SMD-corner fracture type" (DCV/SMD-CF) demonstrated in most reported cases.
Currarino G; Birch JG; Herring JA
Pediatr Radiol; 2000 Jan; 30(1):14-24. PubMed ID: 10663502
[TBL] [Abstract][Full Text] [Related]
13. Unclassified short stature, possibly spondyloepiphyseal dysplasia, possibly multiple epiphyseal dysplasia, in father and daughter.
Elliott DE
Birth Defects Orig Artic Ser; 1974; 10(12):399-405. PubMed ID: 4218780
[No Abstract] [Full Text] [Related]
14. Radiologic findings of Patterson-Lowry rhizomelic dysplasia in two sisters.
Damar Ç; Boyunağa Ö; Derinkuyu BE; Battaloğlu N; Ezgü FS
Skeletal Radiol; 2014 Nov; 43(11):1651-4. PubMed ID: 25037730
[TBL] [Abstract][Full Text] [Related]
15. The treatment of infantile coxa vara with the external circular fixator.
Galante VN; Caiaffa V; Franchin F; Colasuonno R
Ital J Orthop Traumatol; 1990 Dec; 16(4):491-500. PubMed ID: 2099930
[TBL] [Abstract][Full Text] [Related]
16. Further delineation of the 3-M syndrome with review of the literature.
Hennekam RC; Bijlsma JB; Spranger J
Am J Med Genet; 1987 Sep; 28(1):195-209. PubMed ID: 3314510
[TBL] [Abstract][Full Text] [Related]
17. Genu valgum in children with coxa vara resulting from hip disease.
Shim JS; Kim HT; Mubarak SJ; Wenger DR
J Pediatr Orthop; 1997; 17(2):225-9. PubMed ID: 9075101
[TBL] [Abstract][Full Text] [Related]
18. Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies.
Machol K; Jain M; Almannai M; Orand T; Lu JT; Tran A; Chen Y; Schlesinger A; Gibbs R; Bonafe L; Campos-Xavier AB; Unger S; Superti-Furga A; Lee BH; Campeau PM; Burrage LC
Am J Med Genet A; 2017 Mar; 173(3):733-739. PubMed ID: 27888646
[TBL] [Abstract][Full Text] [Related]
19. Infantile coxa vara.
Calhoun JD; Pierret G
Am J Roentgenol Radium Ther Nucl Med; 1972 Jul; 115(3):561-8. PubMed ID: 5038637
[No Abstract] [Full Text] [Related]
20. Does it always have to be Perthes' disease? What is epiphyseal dysplasia?
Hesse B; Kohler G
Clin Orthop Relat Res; 2003 Sep; (414):219-27. PubMed ID: 12966296
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]