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6. Comparative study of sole patterns in chromosomal abnormalities. Penrose LS; Loesch D J Ment Defic Res; 1970 Jun; 14(2):129-40. PubMed ID: 5512213 [No Abstract] [Full Text] [Related]
7. [The importance of configurations or papillary lines in the identification of chromosomal diseases]. Rott HD Folia Clin Int (Barc); 1969 Oct; 19(10):500-6. PubMed ID: 5396731 [No Abstract] [Full Text] [Related]
8. [The chromosomal pathology as a contribution to a genetically oriented psychiatry]. Haberlandt WF Nervenarzt; 1966 Feb; 37(2):45-51. PubMed ID: 4226918 [No Abstract] [Full Text] [Related]
9. Comparison of chromosomal behavior in cultured lymphocytes and fibroblasts from patients with chromosomal disorders and controls. Higurashi M; Conen PE Cytogenetics; 1971; 10(4):273-85. PubMed ID: 5127016 [No Abstract] [Full Text] [Related]
10. Cytogenetic survey of 504 mentally retarded individuals. Singh DN; Osborne RA; Paul JR; Catoe S; Katzberg A; Hennigar GR; Barnett CD J Ment Defic Res; 1974 Dec; 18(4):293-305. PubMed ID: 4282744 [No Abstract] [Full Text] [Related]
11. Neurofibromatosis type 1 with overlap Turner syndrome and Klinefelter syndrome. Hatipoglu N; Kurtoglu S; Kendirci M; Keskin M; Per H J Trop Pediatr; 2010 Feb; 56(1):69-72. PubMed ID: 19578129 [TBL] [Abstract][Full Text] [Related]
14. [Indications for chromosome analysis in childhood]. Goetz P; Kucerová M; Macek M Cesk Pediatr; 1970 Apr; 25(4):161-5. PubMed ID: 4245790 [No Abstract] [Full Text] [Related]
15. [Electroencephalographic reports on the dysmorphic syndrome]. Cavazzuti GB; Gatti G; Tamburino G Riv Neurol; 1975; 45(1):111-7. PubMed ID: 124938 [No Abstract] [Full Text] [Related]
16. "Cri du chat" syndrome. Partial deletion of the short arm of a chromosome No. 5. Report of a case. Hustinx TW; Wijffels JC Maandschr Kindergeneeskd; 1965 Aug; 33(8):286-98. PubMed ID: 5848077 [No Abstract] [Full Text] [Related]
17. [Autoradiographic study of abnormal chromosomes in "Cri du chat" syndrome]. Almeida JC; Barcinski MA; Abreu MC; Mello RS Arq Bras Endocrinol Metabol; 1967 Apr; 16(1):35-7. PubMed ID: 5604082 [No Abstract] [Full Text] [Related]
18. Cri du chat and Turner syndrome features in a newborn girl with an unbalanced 45,X,psu dic(5;X)(p15.2;p22.1) karyotype: FISH and replication banding studies. Reddy KS; Smith DL; Ball CS Ann Genet; 1999; 42(2):105-8. PubMed ID: 10434125 [TBL] [Abstract][Full Text] [Related]
19. [Genetic counseling in cases of genodermatosis]. Kozlowski J; Mazurek A Przegl Dermatol; 1972; 59(5):683-9. PubMed ID: 4265207 [No Abstract] [Full Text] [Related]
20. A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome. Goodart SA; Simmons AD; Grady D; Rojas K; Moyzis RK; Lovett M; Overhauser J Genomics; 1994 Nov; 24(1):63-8. PubMed ID: 7896290 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]