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4. Guide to human chromosome defects. Redding A; Hirshhorn K Birth Defects Orig Artic Ser; 1970 May; 6(1):91-106. PubMed ID: 5522728 [No Abstract] [Full Text] [Related]
5. [Triploidy (69,XXY) in a live born child]. Keutel J; Dollmann A; Münster W Z Kinderheilkd; 1970; 109(2):104-17. PubMed ID: 5494203 [No Abstract] [Full Text] [Related]
6. Gonadal dysgenesis in chromatin-positive patients. Morales A Bol Asoc Med P R; 1974 Nov; 66(11):222-4. PubMed ID: 4532926 [No Abstract] [Full Text] [Related]
7. [Apropos of a translocation of a part of the long arms of a chromosome 5 on the long arms of a chromosome of the D group (Bq-, Dq+)]. Beauvais P; Rumpler Y; Ruch JV; Dreyfus J; Haeberle C Arch Fr Pediatr; 1969; 26(6):695-704. PubMed ID: 5802061 [No Abstract] [Full Text] [Related]
8. [The use of genetic control of the effect of occupational hazards]. Borodkin PA Gig Sanit; 1969 Dec; 34(12):43-6. PubMed ID: 5392970 [No Abstract] [Full Text] [Related]
9. [Systematic study of the Barr body in 500 infants with severe congenital heart diseases]. Gautier M; Nouaille J Arch Fr Pediatr; 1967 Jan; 24(1):109. PubMed ID: 6031448 [No Abstract] [Full Text] [Related]
10. Sex chromosomal anomalies in newborn infants. A 3-year survey of fetal membranes. Mikamo K Obstet Gynecol; 1968 Nov; 32(5):688-99. PubMed ID: 5742485 [No Abstract] [Full Text] [Related]
11. Sex chromatin and chromosome analysis. Runyan JW; Williams DL Med Times; 1967 May; 95(5):512-31. PubMed ID: 5342669 [No Abstract] [Full Text] [Related]
12. Triploidy in man. Report of a case and a discussion on etiology. Schindler AM; Mikamo K Cytogenetics; 1970; 9(2):116-30. PubMed ID: 5461080 [No Abstract] [Full Text] [Related]
13. Prognosis in newborn infants with X-chromosomal abnormalities. Eller E; Frankenburg W; Puck M; Robinson A Pediatrics; 1971 Apr; 47(4):681-8. PubMed ID: 5089757 [No Abstract] [Full Text] [Related]
14. [A case of complete triploidy (69,XXY) in a premature infant. Presence of a clinical syndrome characteristic of this chromosome abnormality]. Castel Y; Rivière D; Toudic L; Alix D; Leroy JP Ann Pediatr (Paris); 1976 Oct; 23(10):639-45. PubMed ID: 16106892 [No Abstract] [Full Text] [Related]
15. [On a case of abnormally long Y chromosome and nuclear formation similar to Barr chromatin]. Carletti B; Kehyayan E Minerva Pediatr; 1968 May; 20(19):1017-20. PubMed ID: 5740607 [No Abstract] [Full Text] [Related]
16. A hermaphrodite with a sex chromatin anomaly. O'Mahony MP J Ir Med Assoc; 1966 Nov; 59(353):151-4. PubMed ID: 5979336 [No Abstract] [Full Text] [Related]
17. Frequency of sex chromosome anomaly among schizophrenic patients. Tsuboi T; Asaka A; Hamada S; Nagumo Y Jinrui Idengaku Zasshi; 1966 Aug; 11(1):39-40. PubMed ID: 6008877 [No Abstract] [Full Text] [Related]
18. Two familial translocations involving the 6-12 group. With meiotic studies in one. McDermott A; Insley J; Rushton DI; Edwards JH Teratology; 1968 May; 1(2):135-51. PubMed ID: 5759133 [No Abstract] [Full Text] [Related]
19. [Sex chromatin and karyotype in primary amenorrhea]. Pardo EA; Costa Bianchi JE; Barata AD; Quaglio HC; Mayo S; Roca D; Baldi EJ Obstet Ginecol Lat Am; 1973; 31(3-4):127-43. PubMed ID: 4806741 [No Abstract] [Full Text] [Related]
20. Structural rearrangement of chromosome 1 and 46, XY-47, XXY mosaicism in a child with a disorder of sex differentiation. Zhukovskii MA; Dzenis IG Sov Genet; 1974 Jul; 8(7):932-6. PubMed ID: 4472605 [No Abstract] [Full Text] [Related] [Next] [New Search]