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.
78 related articles for article (PubMed ID: 1384873)
1. [Computerized analysis in the study of multiple congenital defects connected with chromosome abnormalities: phenotype-karyotypic relations and genetic markers]. Ivanov VI; Levina LIa; Konstantinova LM; Zaiarnyĭ AN; Antonenko VG Vestn Ross Akad Med Nauk; 1992; (4):24-30. PubMed ID: 1384873 [TBL] [Abstract][Full Text] [Related]
2. [Approach to differential diagnosis of clinically related forms of chromosomal pathology using computers]. Antonenko VG; Levina LIa; Konstantinova LM; Zaiarnyĭ AN Pediatriia; 1991; (10):25-9. PubMed ID: 1787996 [TBL] [Abstract][Full Text] [Related]
3. [Partial deletion of the short arm of chromosome 4 (the Wolf-Hirschhorn syndrome) with reference to the neurological and electroencephalographic aspects]. Bonaventura F; Adamoli P; Bernardini E; Branchi M; Siani A; Bonora G Pediatr Med Chir; 1994; 16(4):393-8. PubMed ID: 7816704 [TBL] [Abstract][Full Text] [Related]
4. The Wolf-Hirschhorn (4p-) syndrome. Johnson VP; Mulder RD; Hosen R Clin Genet; 1976 Aug; 10(2NA-NA-760903-760909):104-12. PubMed ID: 954225 [TBL] [Abstract][Full Text] [Related]
8. On the deletion 4p16 Wolf-Hirschhorn syndrome. Rivas F; Hernandez A; Nazara Z; Fragoso R; Olivares N; Rolon A; Cantu JM Ann Genet; 1979; 22(4):228-31. PubMed ID: 317787 [TBL] [Abstract][Full Text] [Related]
9. [The follow-up of a child with a syndrome due to partial deletion of chromosome 3 (p25-pter)]. Tucciarone L; Tomassini A; Colasanti A; Sabbi T; Stella P Minerva Pediatr; 1999; 51(7-8):283-8. PubMed ID: 10634062 [TBL] [Abstract][Full Text] [Related]
11. The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome. Guthrie RD; Aase JM; Asper AC; Smith DW Am J Dis Child; 1971 Nov; 122(5):421-5. PubMed ID: 5129531 [No Abstract] [Full Text] [Related]
12. A practical application of fluorescent in situ hybridization to the Wolf-Hirschhorn syndrome. Fagan K; Colley P; Partington M Pediatrics; 1994 May; 93(5):826-7. PubMed ID: 8165089 [No Abstract] [Full Text] [Related]
13. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat. Qumsiyeh MB; Stevens CA Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287 [TBL] [Abstract][Full Text] [Related]
14. Tetrasomy 9p caused by idic (9) (pter----q13----pter). Cavalcanti DP; Ferrari I; de Almeida JC; de Pina Neto JM; de Oliveira JA Am J Med Genet; 1987 Jul; 27(3):497-503. PubMed ID: 3631125 [TBL] [Abstract][Full Text] [Related]
15. [Computerized diagnosis of syndrome of multiple congenital developmental defects]. Cherstvoĭ ED; Laziuk GI; Krasnoproshin VV; Obraztsov VA Pediatriia; 1982 Jul; (7):41-3. PubMed ID: 7133872 [No Abstract] [Full Text] [Related]
16. [Phenotype and "critical segments" of chromosomes during partial aneuploidy for chromosome 4 in man]. Ivanov VI; Levina LIa; Konstantinova LM; Zaiarnyĭ AN; Kuleshov NP Genetika; 1990 May; 26(5):912-24. PubMed ID: 2397885 [TBL] [Abstract][Full Text] [Related]
17. Ring chromosome 15 syndrome. Fryns JP; Jaeken J; Devlieger H; Debucquoy P; Eggermont E; Van den Berghe H Acta Paediatr Belg; 1981; 34(1):47-9. PubMed ID: 7270144 [No Abstract] [Full Text] [Related]
18. Chromosomal abnormalities and glaucoma: a case of congenital glaucoma associated with 9p deletion syndrome. Saha K; Lloyd IC; Russell-Eggitt IM; Taylor DS Ophthalmic Genet; 2007 Jun; 28(2):69-72. PubMed ID: 17558847 [TBL] [Abstract][Full Text] [Related]
19. Application of fluorescence in situ hybridization to the identification of different marker chromosomes. Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644 [TBL] [Abstract][Full Text] [Related]
20. The Wolf-Hirschhorn syndrome. Deletion of the short arm of chromosome 4. Fryns JP; François B; Timmermans J; Emmery L; Speybrouck J; Van Den Berghe H Acta Paediatr Belg; 1979; 32(2):135-9. PubMed ID: 495091 [No Abstract] [Full Text] [Related] [Next] [New Search]