131 related articles for article (PubMed ID: 11146473)
1. Scapuloiliac dysostosis (Kosenow syndrome, pelvis-shoulder dysplasia) spectrum: three additional cases.
Elliott AM; Roeder ER; Witt DR; Rimoin DL; Lachman RS
Am J Med Genet; 2000 Dec; 95(5):496-506. PubMed ID: 11146473
[TBL] [Abstract][Full Text] [Related]
2. Autosomal dominant inheritance of scapuloiliac dysostosis.
Amor DJ; Savarirayan R; Bankier A; Jensen F; Hauser SP
Am J Med Genet; 2000 Dec; 95(5):507-9. PubMed ID: 11146474
[No Abstract] [Full Text] [Related]
3. Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome.
Dikoglu E; Simsek-Kiper PO; Utine GE; Campos-Xavier B; Boduroglu K; Bonafé L; Superti-Furga A; Unger S
Am J Med Genet A; 2013 Dec; 161A(12):3161-5. PubMed ID: 24039145
[TBL] [Abstract][Full Text] [Related]
4. Pelvis-shoulder dysplasia.
Hauser SE; Chemke JM; Bankier A
Pediatr Radiol; 1998 Sep; 28(9):681-2. PubMed ID: 9732492
[TBL] [Abstract][Full Text] [Related]
5. Scapuloiliac dysostosis.
Blane CE; Holt JF; Vine AK
Br J Radiol; 1984 Jun; 57(678):526-8. PubMed ID: 6426572
[No Abstract] [Full Text] [Related]
6. [Pelvis-shoulder dysplasia].
Kosenow W; Niederle J; Sinios A
Fortschr Geb Rontgenstr Nuklearmed; 1970 Jul; 113(1):39-48. PubMed ID: 4994116
[No Abstract] [Full Text] [Related]
7. Miller postaxial acrofacial dysostosis syndrome. Follow-up data of a family and confirmation of autosomal recessive inheritance.
Chrzanowska K; Fryns JP
Clin Genet; 1993 May; 43(5):270. PubMed ID: 8375109
[No Abstract] [Full Text] [Related]
8. Thoracic-pelvic dysostosis.
Marik I; Grochova J; Kozlowski K
Clin Dysmorphol; 2000 Oct; 9(4):285-7. PubMed ID: 11045587
[TBL] [Abstract][Full Text] [Related]
9. Acrofacial dysostosis with ambiguous genitalia.
Wulfsberg EA; Curtis J; Wiswell TE; Puntel RA; Levin SW
Am J Med Genet; 1990 Nov; 37(3):384-7. PubMed ID: 2260569
[TBL] [Abstract][Full Text] [Related]
10. Developmental anomalies of the scapula-the "omo"st forgotten bone.
Williams MS
Am J Med Genet A; 2003 Aug; 120A(4):583-7. PubMed ID: 12884444
[TBL] [Abstract][Full Text] [Related]
11. Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndrome.
Petit P; Moerman P; Fryns JP
Am J Med Genet; 1992 Feb; 42(3):343-5. PubMed ID: 1536176
[TBL] [Abstract][Full Text] [Related]
12. Spondylocostal dysostosis: dominant type.
Lorenz P; Rupprecht E
Am J Med Genet; 1990 Feb; 35(2):219-21. PubMed ID: 2309760
[TBL] [Abstract][Full Text] [Related]
13. Bilateral dysplasia of the neck of scapula and associated anomalies.
Pettersson H
Acta Radiol Diagn (Stockh); 1981; 22(1):81-4. PubMed ID: 7257856
[TBL] [Abstract][Full Text] [Related]
14. Osteopathia striata with cranial sclerosis: highly variable phenotypic expression within a family.
Savarirayan R; Nance J; Morris L; Haan E; Couper R
Clin Genet; 1997 Oct; 52(4):199-205. PubMed ID: 9383023
[TBL] [Abstract][Full Text] [Related]
15. An unusual case of caudal duplication.
Surendran N; Nainan KM; Paulose MO
J Pediatr Surg; 1986 Nov; 21(11):924-5. PubMed ID: 3794939
[TBL] [Abstract][Full Text] [Related]
16. New lethal acrofacial dysostosis syndrome.
Hecht JT
Am J Med Genet; 1992 Feb; 42(3):400-1. PubMed ID: 1536191
[No Abstract] [Full Text] [Related]
17. Complete bilateral agenesis of the ilium in a 7-year-old ambulatory girl: case report.
Mac-Thiong JM; Leduc S; Labelle H
Spine (Phila Pa 1976); 2005 Jul; 30(14):E420-3. PubMed ID: 16025020
[TBL] [Abstract][Full Text] [Related]
18. Identical twins with an autosomal recessive form of spondylocostal dysostosis.
Satar M; Kozanoglu MN; Atilla E
Clin Genet; 1992 Jun; 41(6):290-2. PubMed ID: 1623623
[TBL] [Abstract][Full Text] [Related]
19. An unusual form of caudal duplication (dipygus).
Chadha R; Dhar A; Bagga D; Malhotra CJ; Taneja SB
J Pediatr Surg; 1993 May; 28(5):728-30. PubMed ID: 8340869
[TBL] [Abstract][Full Text] [Related]
20. Further evidence for causation of ischiospinal dysostosis by a pathogenic variant in BMPER and expansion of the phenotype.
Salian S; Nampoothiri S; Shukla A; Girisha KM
Congenit Anom (Kyoto); 2019 Jan; 59(1):26-27. PubMed ID: 29704261
[No Abstract] [Full Text] [Related]
[Next] [New Search]