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3. Cytogenetics and the pathologist. Carr DH Pathol Annu; 1975; 10():93-144. PubMed ID: 126409 [No Abstract] [Full Text] [Related]
4. 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]
5. II. A review of clinical syndromes associated with aberrations of the autosomes. Williams JD; Summitt RL J Tenn Med Assoc; 1971 Apr; 64(4):310-7. PubMed ID: 4252589 [No Abstract] [Full Text] [Related]
10. [Indications for chromosome analysis from the pediatric viewpoint]. Steinbicker V; Braun HS; Hemke G; Euchler HB Kinderarztl Prax; 1973 Feb; 41(2):91-8. PubMed ID: 4267824 [No Abstract] [Full Text] [Related]
11. De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation. Chaganti RS; Morillo-Cucci G; Friis L; Degnan M; German J Ann Genet; 1976 Mar; 19(1):43-8. PubMed ID: 1084121 [TBL] [Abstract][Full Text] [Related]
12. Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocation. Leisti J; Kaback MM; Rimoin DL Birth Defects Orig Artic Ser; 1975; 11(5):317-9. PubMed ID: 1218232 [No Abstract] [Full Text] [Related]
15. Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect. Petit P; Fryns JP Genet Couns; 1990; 1(2):179-84. PubMed ID: 2081002 [TBL] [Abstract][Full Text] [Related]
16. Updating advances in cytogenetics. Applications of the new chromosome banding methods. Breg WR Birth Defects Orig Artic Ser; 1974; 10(8):7-18. PubMed ID: 4142402 [No Abstract] [Full Text] [Related]
17. 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]
18. [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]
19. [Familial segregation of a t(5p-;13q+). Complementary analysis from specimens preserved in liquid nitrogen]. Carpentier S; Dutrillaux B; Lafourcade J; Berger R; Rethoré MO; Lejeune J Ann Genet; 1972 Mar; 15(1):57-60. PubMed ID: 4537617 [No Abstract] [Full Text] [Related]
20. [Cytogenetic examination in gynecology and obstetrics]. Knörr K Med Klin; 1974 Jan; 69(3):75-82. PubMed ID: 4274010 [No Abstract] [Full Text] [Related] [Next] [New Search]