These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
170 related articles for article (PubMed ID: 6431894)
1. [The r(14) syndrome. 3 new observations]. Gilgenkrantz S; Morali A; Vidailhet M; Saura R; Serville F; Fontan D; Moraine C Ann Genet; 1984; 27(2):73-8. PubMed ID: 6431894 [TBL] [Abstract][Full Text] [Related]
2. [Ring chromosome 14. I. A case report on homogeneous r(14)]. Raoul O; Razavi F; Lescs MC; Bouhanna A Ann Genet; 1984; 27(2):88-90. PubMed ID: 6331795 [TBL] [Abstract][Full Text] [Related]
3. [Ring chromosome 14. II. A case report of r(14) mosaicism. The r(14) phenotype]. Rethoré MO; Caille B; Huet de Barochez Y; de Blois MC; Ravel A; Lejeune J Ann Genet; 1984; 27(2):91-5. PubMed ID: 6331796 [TBL] [Abstract][Full Text] [Related]
4. Ring chromosome 16: a new case. Vianello MG; Cottafava F; Bartoli D; Franzone G; Casazzava R; Gastaldi R Ann Genet; 1990; 33(1):36-9. PubMed ID: 2195979 [TBL] [Abstract][Full Text] [Related]
7. Multiple critical smallest region of overlap in monosomy 16Q syndrome? Doco-Fenzy M; Elchardus JF; Brami G; Digeon B; Gruson N; Adnet JJ Genet Couns; 1994; 5(1):39-44. PubMed ID: 8031534 [TBL] [Abstract][Full Text] [Related]
8. Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome in two siblings: further delineation of the syndrome and review of the literature. Krajewska-Walasek M Genet Couns; 1994; 5(4):345-55. PubMed ID: 7888136 [TBL] [Abstract][Full Text] [Related]
9. Antley-Bixler syndrome: case report and review of the literature. Poddevin F; Delobel B; Courreges P; Bayart M Genet Couns; 1995; 6(3):241-6. PubMed ID: 8588853 [TBL] [Abstract][Full Text] [Related]
12. [ICF syndrome. Immunodeficiency, chromosomal centromere instability, facial anomalies. Case report and literature review]. Kieback P; Wendisch H; Lorenz P; Hinkel K Monatsschr Kinderheilkd; 1992 Feb; 140(2):91-4. PubMed ID: 1557060 [TBL] [Abstract][Full Text] [Related]
13. [Vitreoretinal changes in siblings of two patients with Stickler syndrome. Study of two families]. Langmann A; Langmann G; Kainer U; Faulborn J Ophthalmologe; 1993 Oct; 90(5):506-9. PubMed ID: 8219641 [TBL] [Abstract][Full Text] [Related]
14. Prenatal detection of de novo inversion of chromosome (2) (p13q11.2) and postnatal follow-up. Kozma C; Subasinghe C; Meck J Prenat Diagn; 1996 Apr; 16(4):366-70. PubMed ID: 8734815 [TBL] [Abstract][Full Text] [Related]
15. Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype. Lahn BT; Ma N; Breg WR; Stratton R; Surti U; Page DC Nat Genet; 1994 Nov; 8(3):243-50. PubMed ID: 7874166 [TBL] [Abstract][Full Text] [Related]
16. Classification, etiology, and genetic aspects of craniofacial anomalies. Kaye CI Otolaryngol Clin North Am; 1981 Nov; 14(4):827-64. PubMed ID: 7335360 [TBL] [Abstract][Full Text] [Related]
17. Infant male with ring chromosome 14. Triolo O; Serra A; Bova R; Carlo Stella N; Caruso P Ann Genet; 1981; 24(4):236-8. PubMed ID: 6977306 [No Abstract] [Full Text] [Related]
18. Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome. Goddeeris P; Fryns JP; van den Berghe H J Genet Hum; 1980 Mar; 28(1):57-60. PubMed ID: 7400786 [TBL] [Abstract][Full Text] [Related]
19. Mosaic 5p tetrasomy. Stanley WS; Powell CM; Devine GC; Ellingham T; Samango-Sprouse CA; Vaught DR; Murphy BA; Rosenbaum KN Am J Med Genet; 1993 Mar; 45(6):774-6. PubMed ID: 8456861 [TBL] [Abstract][Full Text] [Related]
20. [Congenital dwarfisms with dysmorphism. 1. Congenital dwarfism with craniofacial dysmorphism and body asymmetry (Silver-Russel type)]. Anoussakis C; Karpathios T; Zervos N; Liakakos D Pediatrie; 1974; 29(3):249-59. PubMed ID: 4438032 [No Abstract] [Full Text] [Related] [Next] [New Search]