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43. On the biologic nature of associations: evidence from a study of radial ray deficiencies and associated malformations. Evans JA; Vitez M; Czeizel A Birth Defects Orig Artic Ser; 1993; 29(1):63-81. PubMed ID: 8280894 [No Abstract] [Full Text] [Related]
44. Congenital anal anomalies in two families with the Opitz G syndrome. Tolmie JL; Coutts N; Drainer IK J Med Genet; 1987 Nov; 24(11):688-91. PubMed ID: 3430544 [TBL] [Abstract][Full Text] [Related]
45. Complex structural rearrangement of chromosomes 7, 10, 14 and 21. de Asis ML; Saito F; Tonomura A Jinrui Idengaku Zasshi; 1984 Dec; 29(4):453-9. PubMed ID: 6535858 [No Abstract] [Full Text] [Related]
46. Full monosomy 21: a clinically recognizable syndrome? Fryns JP; D'Hondt F; Goddeeris P; van den Berghe H Hum Genet; 1977 Jun; 37(2):155-9. PubMed ID: 885536 [TBL] [Abstract][Full Text] [Related]
47. The syndrome associated with the partial D-monosomy. Case report and review. Orbeli DJ; Lurie IW; Goroshenko JL Humangenetik; 1971; 13(4):296-308. PubMed ID: 5135849 [No Abstract] [Full Text] [Related]
49. Chromosomal abnormalities of the E group and surgical anomalies in neonates. Grosfeld JL; Kontras SB; Sommer A Surgery; 1971 Mar; 69(3):451-5. PubMed ID: 5101694 [No Abstract] [Full Text] [Related]
53. Fluorescence in situ hybridisation on formalin fixed fetal tissue in the diagnosis of chromosomal syndromes. Cobben JM; Essed CE; Hirdes J; Kraayenbrink RA; Van der Veen A Genet Couns; 1994; 5(2):141-5. PubMed ID: 7917121 [TBL] [Abstract][Full Text] [Related]
54. [Genetic counseling. Apropos of familial transmission of 21-D translocation]. Attal B; Cottin J; Someily I Bull Fed Soc Gynecol Obstet Lang Fr; 1971; 23(4):494-7. PubMed ID: 5153258 [No Abstract] [Full Text] [Related]
56. Human chromosomal deletion: two patients with the 4p- syndrome. Arias D; Passarge E; Engle MA; German J J Pediatr; 1970 Jan; 76(1):82-8. PubMed ID: 5410164 [No Abstract] [Full Text] [Related]
57. Typical and partial cat eye syndrome: identification of the marker chromosome by FISH. Liehr T; Pfeiffer RA; Trautmann U Clin Genet; 1992 Aug; 42(2):91-6. PubMed ID: 1424237 [TBL] [Abstract][Full Text] [Related]
58. [Identification of an unusual chromosome anomaly in a malformative syndrome]. Vianello MG; De Prà M Minerva Pediatr; 1969 Apr; 21(15):611-8. PubMed ID: 5402255 [No Abstract] [Full Text] [Related]
59. Anal atresia and abdominal wall defect as unusual symptoms in EEC syndrome. De Smet L; Fryns JP Genet Couns; 1995; 6(2):127-30. PubMed ID: 7546455 [TBL] [Abstract][Full Text] [Related]
60. A chromosome No. 2 abnormality in a child with a few congenital defects. Escobar JI; Lakatua DJ; Streifel B; Virnig NL; Sanchez O Clin Genet; 1977 Jan; 11(1):8-12. PubMed ID: 830454 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]