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.
8. [Monosomy 21 with mosaicism 45,XX,21--46,XX,21 pi]. Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R Arch Fr Pediatr; 1970; 27(10):1069-79. PubMed ID: 5495707 [No Abstract] [Full Text] [Related]
9. Clinical, cytogenetic and autoradiographic studies in 10 cases with rare chromosome disorders II. Cases 3,4 and 5. Moore MK; Engel E Ann Genet; 1970 Jun; 13(2):129-34. PubMed ID: 5310697 [No Abstract] [Full Text] [Related]
10. [13-15 trisomy in mosaicism]. Scouras J; Cuendet JF; Catti A Bull Mem Soc Fr Ophtalmol; 1972; 85(0):91-100. PubMed ID: 4211746 [No Abstract] [Full Text] [Related]
11. Autosomal chromosome aberrations. A review of the clinical syndromes caused by structural chromosome aberrations, mosaic-trisomies 8 and 9, and triploidy. Schinzel A Ergeb Inn Med Kinderheilkd; 1976; 38():37-94. PubMed ID: 782877 [No Abstract] [Full Text] [Related]
12. [Ocular manifestations of trisomy 18]. Ardouin M; Urvoy M; Lautridou A; Le Marec B; Senecal J Arch Ophtalmol Rev Gen Ophtalmol; 1972; 32(6):457-76. PubMed ID: 4264548 [No Abstract] [Full Text] [Related]
13. Cat-eye syndrome: evaluation of the extra chromosome with banding techniques. Case report. De Chieri R; Malfatti C; Stanchi F; Albores JM J Genet Hum; 1974 Jun; 22(2):101-7. PubMed ID: 4213897 [No Abstract] [Full Text] [Related]
14. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies. Oikawa K; Kajii T; Shimba H; Sasaki M Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379 [No Abstract] [Full Text] [Related]
15. [Dermatoglyphics in medicine]. Sharets IuD Vestn Akad Med Nauk SSSR; 1973; 28(7):61-9. PubMed ID: 4274403 [No Abstract] [Full Text] [Related]
16. [A chemical and karyological study in a case of dyscraniotic oligophrenia]. Caldarini G; Paracchi G Folia Hered Pathol (Milano); 1968 Jul; 17(3):103-12. PubMed ID: 5732581 [No Abstract] [Full Text] [Related]
17. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters]. Giovannelli G; Forabosco A; Dutrillaux B Ann Genet; 1974 Jun; 17(2):119-24. PubMed ID: 4547939 [No Abstract] [Full Text] [Related]
18. [Apropos of trisomy 18 - a study of 4 observations]. Gilgenkrantz S; Sapelier J; Thiriet M; Kahn C; Pierson M Ann Genet; 1967 Mar; 10(1):32-8. PubMed ID: 5300124 [No Abstract] [Full Text] [Related]
19. Dermatoglyphic patterns and clinical diagnosis by discriminant function. Penrose LS; Loesch D Ann Hum Genet; 1971 Jul; 35(1):51-60. PubMed ID: 5571746 [No Abstract] [Full Text] [Related]
20. [Trisomy 9p : 2 further cases]. Turleau C; de Grouchy J; Chavin-Colin F; Roubin M; Langmaid H Ann Genet; 1974 Sep; 17(3):167-74. PubMed ID: 4548817 [No Abstract] [Full Text] [Related] [Next] [New Search]