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.
90 related articles for article (PubMed ID: 5997386)
1. [Multiple congenital malformations in a child with an extrachromosome in the G group]. Vianello MG; Cinque NA; Loiodice G Pathologica; 1966; 58(867):537-40. PubMed ID: 5997386 [No Abstract] [Full Text] [Related]
2. [Diagnosis of Edwards syndrome in newborns]. Dunin-Wasowicz D; Krajewska-Walasek M; Rowecka-Trzebicka K; Gurkau-Malecha M; Gutkowska A; Chrzanowska K Pediatr Pol; 1995 Oct; 70(10):865-74. PubMed ID: 8649934 [TBL] [Abstract][Full Text] [Related]
3. Trisomy 22 confirmed by fluorescent in situ hybridization. Stratton RF; DuPont BR; Mattern VL; Young RS; McCourt JW; Moore CM Am J Med Genet; 1993 Apr; 46(1):109-12. PubMed ID: 8494030 [TBL] [Abstract][Full Text] [Related]
5. Picture of the month. Smith-Lemli-Opitz syndrome. Gellis SS; Feingold M Am J Dis Child; 1968 May; 115(5):603-4. PubMed ID: 5689489 [No Abstract] [Full Text] [Related]
6. Tandem duplication of chromosome 14 (q24 leads to q32) in male newborn with congenital malformations. Nikolis J; Ivanović K; Kosanović M Clin Genet; 1983 Apr; 23(4):321-4. PubMed ID: 6851224 [TBL] [Abstract][Full Text] [Related]
7. A case of lateral facial clefts with Fallot tetralogy, duodenal stenosis and intestinal malrotation: a new multiple congenital anomaly syndrome? Kumar D Clin Dysmorphol; 1999 Jan; 8(1):19-21. PubMed ID: 10327247 [TBL] [Abstract][Full Text] [Related]
8. [Rubinstein-Taybi syndrome in a 2-year-old boy]. Bartkowiak K; Olejniczakowa T Pediatr Pol; 1968 May; 43(5):637-40. PubMed ID: 5669065 [No Abstract] [Full Text] [Related]
9. [Trisomy 20p]. Zergollern L; Begović D Acta Med Iugosl; 1984; 38(1):69-75. PubMed ID: 6711357 [No Abstract] [Full Text] [Related]
10. [Maternal translocation t (1; 8; 15) and trisomy 8 qter in her daughter. Genetic counseling]. Ballesta F; Fernández E; Milá M J Genet Hum; 1980 Sep; 28(3):361-6. PubMed ID: 7463035 [No Abstract] [Full Text] [Related]
11. [Smith-Lemli-Opitz syndrome. Case report and differential diagnosis]. Domenici R; Fiorini V; Giorgi F Minerva Pediatr; 1982 Sep; 34(17):709-14. PubMed ID: 6292682 [No Abstract] [Full Text] [Related]
12. Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: specific entity or variant of a described condition? Göhlich-Ratmann G; Lackner A; Schaper J; Voit T; Gillessen-Kaesbach G Am J Med Genet; 2000 Nov; 95(3):241-6. PubMed ID: 11102931 [TBL] [Abstract][Full Text] [Related]
13. Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome. Jardine PE; Burvill-Holmes LC; Schutt WH; Lunt PW Clin Dysmorphol; 1993 Jul; 2(3):269-73. PubMed ID: 8287190 [TBL] [Abstract][Full Text] [Related]
14. Type III tracheal agenesis with familial tetralogy of Fallot and absent pulmonary valve syndrome. Hirt-Armon K; Pober BR; Holmes LB Am J Med Genet; 1996 Nov; 65(4):266-8. PubMed ID: 8923932 [TBL] [Abstract][Full Text] [Related]
15. Trisomy 18 with multiple rare malformations: report of one case. Su PH; Chen JY; Hsu CH; Chen SJ; Chan SW; Lin LL Acta Paediatr Taiwan; 2007; 48(5):272-5. PubMed ID: 18254577 [TBL] [Abstract][Full Text] [Related]