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.
23. [Bilateral irido-chorio-retinal coloboma in a case of ringed chromosome 18]. Brihaye M; Farnir A; Poncelet M; Petit P Bull Soc Belge Ophtalmol; 1969 Nov; 153():696-701. PubMed ID: 4992558 [No Abstract] [Full Text] [Related]
24. Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18. Fraccaro M; Herin P; Hultén M; Ivemark BI; Jonasson J; Lindsten J; Tiepolo L; Zetterqvist P Ann Genet; 1972 Jun; 15(2):93-8. PubMed ID: 4537728 [No Abstract] [Full Text] [Related]
29. Tandem duplication of proximal 22q: a cause of cat-eye syndrome. Reiss JA; Weleber RG; Brown MG; Bangs CD; Lovrien EW; Magenis RE Am J Med Genet; 1985 Jan; 20(1):165-71. PubMed ID: 3970068 [TBL] [Abstract][Full Text] [Related]
30. [Crying cat syndrome discovered during a routine examination]. Lafon R; Emberger JM; Pouget R; Chiariny JF Ann Med Psychol (Paris); 1972; 2(3):431-8. PubMed ID: 4675135 [No Abstract] [Full Text] [Related]
31. Multiple congenital defects associated with trisomy for the short arm of chromosome 4. Owen L; Martin B; Blank CE; Harris F J Med Genet; 1974 Sep; 11(3):291-5. PubMed ID: 4431034 [TBL] [Abstract][Full Text] [Related]
32. [Minor ocular manifestations in a case of D trisomy by 13-14 translocation. Coloboma of the iris, congenital retinal fold, without microphthalmia or choroid coloboma]. Seringe P; Dhermy P; Loewe-Lyon S; Despres P; Aron JJ Arch Ophtalmol Rev Gen Ophtalmol; 1971; 31(6):497-516. PubMed ID: 4255267 [No Abstract] [Full Text] [Related]
33. [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]
34. [A case of annular chromosome 9. Indentification by controlled denaturation]. Fraisse J; Lauras B; Ooghe MJ; Freycon F; Rethoré MO Ann Genet; 1974 Sep; 17(3):175-80. PubMed ID: 4548818 [No Abstract] [Full Text] [Related]
35. [Ocular abnormalities of phenotype DR (ring D chromosome)]. Saraux H; Réthoré MO; Aussannaire M; Dhermy P; Joly C; Le Loch J; Praud E; Lejeune J Ann Ocul (Paris); 1970 Aug; 203(8):737-48. PubMed ID: 4992291 [No Abstract] [Full Text] [Related]
36. [Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)]. Rethoré MO; Dutrillaux B; Job JC; Lejeune J Ann Genet; 1974 Jun; 17(2):109-14. PubMed ID: 4547937 [No Abstract] [Full Text] [Related]
37. [Proceedings: Familial translocation 8-12 and the multiple abnormalities syndrome]. Cousin J; Savary JB; Bayart M; Pauli A; Deminatti M; Fournier A Pediatrie; 1975; 30(3):314. PubMed ID: 1178259 [No Abstract] [Full Text] [Related]
38. [Dermatoglyphics in medicine]. Sharets IuD Vestn Akad Med Nauk SSSR; 1973; 28(7):61-9. PubMed ID: 4274403 [No Abstract] [Full Text] [Related]
40. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution. Hustinx TW; Haar BG; Scheres JM; Rutten FJ Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]