117 related articles for article (PubMed ID: 10649806)
1. Axial mesodermal dysplasia complex: a new case with parental consanguinity.
Mota CR; Azevedo M; Rocha G; Manuela F; Coelho R; Lima MR
Clin Dysmorphol; 2000 Jan; 9(1):73-5. PubMed ID: 10649806
[TBL] [Abstract][Full Text] [Related]
2. Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC).
Bergmann C; Zerres K; Peschgens T; Senderek J; Hörnchen H; Rudnik-Schöneborn S
Am J Med Genet A; 2003 Aug; 121A(2):151-5. PubMed ID: 12910495
[TBL] [Abstract][Full Text] [Related]
3. Axial mesodermal dysplasia spectrum: variable symptoms in affected sibs.
Fryns JP; Remans PJ; Fabry G
Am J Med Genet; 1993 Jul; 46(6):736. PubMed ID: 8362924
[No Abstract] [Full Text] [Related]
4. Report of a new case of axial mesodermal dysplasia complex.
Bini R; Danti DA; Materassi M; Pela I
Clin Genet; 1996 Nov; 50(5):407-10. PubMed ID: 9007333
[TBL] [Abstract][Full Text] [Related]
5. The oculoauriculovertebral dysplasia syndrome of Goldenhar.
Sugar HS
Am J Ophthalmol; 1966 Oct; 62(4):678-82. PubMed ID: 4959237
[No Abstract] [Full Text] [Related]
6. A patient with VACTERL association, amelia and hemifacial microsomia.
Aftimos S; Winship I
Clin Dysmorphol; 1999 Apr; 8(2):135-7. PubMed ID: 10319203
[TBL] [Abstract][Full Text] [Related]
7. New case of axial mesodermal dysplasia spectrum.
Saraiva JM
Am J Med Genet; 1995 Jan; 55(3):391. PubMed ID: 7726243
[No Abstract] [Full Text] [Related]
8. Axial Mesodermal Dysplasia Complex with a Unique Abnormal Course of Vestibulocochlear Nerve.
Tok Umay S; Özgür A; Görür K; Kömür M; Balcı Y
J Int Adv Otol; 2019 Aug; 15(2):317-320. PubMed ID: 30431015
[TBL] [Abstract][Full Text] [Related]
9. Severe fatal course of axial mesodermal dysplasia spectrum associated with complex cardiac defect in an infant of a mother with insulin dependent diabetes.
Dinleyici EC; Tekin N; Dinleyici M; Kilic Z; Adapinar B; Aksit MA
Am J Med Genet A; 2007 Sep; 143A(18):2156-9. PubMed ID: 17676608
[TBL] [Abstract][Full Text] [Related]
10. [Oculoauriculovertebral dysplasia (author's transl)].
Wagner IU; Wimmer M; Probst P
Klin Padiatr; 1978 Mar; 190(2):209-13. PubMed ID: 417212
[TBL] [Abstract][Full Text] [Related]
11. Epiphyseal, vertebral, and ear (EVE) dysplasia: a new syndrome?
Amiel J; Cormier-Daire V; Journeau P; Mussat P; Munnich A; Lyonnet S
J Med Genet; 1999 Jul; 36(7):561-4. PubMed ID: 10424819
[TBL] [Abstract][Full Text] [Related]
12. Severe axial mesodermal dysplasia spectrum in an infant of a diabetic mother.
Depraetere M; Dehauwere R; Mariën P; Fryns JP
Genet Couns; 1995; 6(4):303-7. PubMed ID: 8775416
[TBL] [Abstract][Full Text] [Related]
13. [The oculo-oto-vertebral syndrome (author's transl)].
Müller WD; Stern E
Klin Padiatr; 1977 Nov; 189(6):417-22. PubMed ID: 414017
[TBL] [Abstract][Full Text] [Related]
14. Rokitansky sequence in association with the facio-auriculo-vertebral sequence: part of a mesodermal malformation spectrum?
Wulfsberg EA; Grigbsy TM
Am J Med Genet; 1990 Sep; 37(1):100-2. PubMed ID: 2240024
[TBL] [Abstract][Full Text] [Related]
15. A distinct skeletal dysplasia in an infant from consanguineous parents.
Cantú JM; Manzano C; Pagán P; García-Cruz D; Hernández A
Birth Defects Orig Artic Ser; 1977; 13(3B):139-47. PubMed ID: 890089
[TBL] [Abstract][Full Text] [Related]
16. [Familial infantile nephrotic syndrome with ocular abnormalities].
Glastre C; Cochat P; Colon S; Bouvier R; Cottin X; Giffon D; Wright C; Dijoud F; David L
Pediatrie; 1989; 44(7):555-8. PubMed ID: 2812971
[TBL] [Abstract][Full Text] [Related]
17. Clinical anophthalmia, dextrocardia, and skeletal anomalies in an infant born to consanguineous parents.
Aughton DJ
Am J Med Genet; 1990 Oct; 37(2):178-81. PubMed ID: 2248283
[No Abstract] [Full Text] [Related]
18. [On a case of Goldehar's syndrome].
Loffredo A; Colaci C; De Luca M; Bongiorno A
Ann Ottalmol Clin Ocul; 1967 Dec; 93(12):1466-76. PubMed ID: 4974469
[No Abstract] [Full Text] [Related]
19. Ophthalmological, skeletal, and cardiac abnormalities in sibs born to consanguineous parents: a new syndrome?
dos Santos Rde C; Castro NH; Ferraz OP; Walter-Moura J; Mustachi Z; Pagnan NA; Gollop TR
Am J Med Genet; 1992 Aug; 43(6):946-8. PubMed ID: 1415344
[TBL] [Abstract][Full Text] [Related]
20. Muscle involvement in Walker-Warburg syndrome. Clinicopathologic features of four cases.
Lichtig C; Ludatscher RM; Mandel H; Gershoni-Baruch R
Am J Clin Pathol; 1993 Nov; 100(5):493-6. PubMed ID: 8249887
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]