Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- CRAIG A. P., SCHTEINGART D. E., SHAW M. W. GONADAL DYSGENESIS WITH XUXX MOSAICISM AND A POSITIVE SEX CHROMATIN PATTERN. J Clin Endocrinol Metab. 1963 Aug;23:752–758. doi: 10.1210/jcem-23-8-752. [DOI] [PubMed] [Google Scholar]
- DEWHURST C. J., PAINE C. G., BLANK C. E. AN XY FEMALE WITH ABSENT GONADS AND VESTIGIAL PELVIC ORGANS. J Obstet Gynaecol Br Commonw. 1963 Aug;70:675–680. doi: 10.1111/j.1471-0528.1963.tb04966.x. [DOI] [PubMed] [Google Scholar]
- FERGUSON-SMITH M. A., JOHNSTON A. W. Chromosome abnormalities in certain diseases of man. Ann Intern Med. 1960 Aug;53:359–371. doi: 10.7326/0003-4819-53-2-359. [DOI] [PubMed] [Google Scholar]
- FERRIER P., GARTLER S. M., WAXMAN S. H., SHEPARD T. H., 2nd Abnormal sexual development associated with sex chromosome mosaicism. Report of three cases. Pediatrics. 1962 May;29:703–713. [PubMed] [Google Scholar]
- FORD C. E., HAMERTON J. L. The chromosomes of man. Nature. 1956 Nov 10;178(4541):1020–1023. doi: 10.1038/1781020a0. [DOI] [PubMed] [Google Scholar]
- FORD C. E., JONES K. W., POLANI P. E., DE ALMEIDA J. C., BRIGGS J. H. A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome). Lancet. 1959 Apr 4;1(7075):711–713. doi: 10.1016/s0140-6736(59)91893-8. [DOI] [PubMed] [Google Scholar]
- FORTEZA G., BONILLA F., BAGUENA R., MONMENEU S., GALBIS M., ZARAGOZA V. [A case of chromatin-negative XY-XX mosaicism with gonadal dysgenesis and female phenotype sex]. Rev Clin Esp. 1963 Mar 31;88:394–398. [PubMed] [Google Scholar]
- FRACCARO M., BOTT M. G., SALZANO F. M., RUSSELL R. W., CRANSTON W. I. Triple chromosomal mosaic in a woman with clinical evidence of a masculinisation. Lancet. 1962 Jun 30;1(7244):1379–1381. doi: 10.1016/s0140-6736(62)92489-3. [DOI] [PubMed] [Google Scholar]
- FUTTERWEIT W., CHAPMAN M. L., SALVANESCHI J. P., MOLOSHOK R. E. Multiple congenital defects in a twelve year old boy with cryptorchidism--"male Turner's syndrome". Metabolism. 1961 Dec;10:1074–1084. [PubMed] [Google Scholar]
- GAGNON J., KATYK-LONGTIN N., SINNOTT J. C. [The syndrome of multiple malformations associated with gonadal dysgenesis (Turner syndrome) with XO chromosome formula]. Union Med Can. 1960 Oct;89:1227–1237. [PubMed] [Google Scholar]
- HADDAD H. M., WILKINS L. Congenital anomalies associated with gonadal aplasia; review of 55 cases. Pediatrics. 1959 May;23(5):885–902. [PubMed] [Google Scholar]
- HAMERTON J. L., JAGIELLO G. M., KIRMAN B. H. Sex-chromosome abnormalities in a population of mentally defective children. Br Med J. 1962 Jan 27;1(5273):220–223. doi: 10.1136/bmj.1.5273.220. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HAYWARD M. D., CAMERON A. H. Triple mosaicism of the sex chromosomes in Turner's syndrome and Hirschsprung's disease. Lancet. 1961 Sep 16;2(7203):623–627. doi: 10.1016/s0140-6736(61)90307-5. [DOI] [PubMed] [Google Scholar]
- JOHNSTON A. W., FERGUSON-SMITH M. A., HANDMAKER S. D., JONES H. W., JONES G. S. The triple-X syndrome. Clinical, pathological, and chromosomal studies in three mentally retarded cases. Br Med J. 1961 Oct 21;2(5259):1046–1052. doi: 10.1136/bmj.2.5259.1046. [DOI] [PMC free article] [PubMed] [Google Scholar]
- JONES H. W., Jr, FERGUSON-SMITH M. A., HELLER R. H. THE PATHOLOGY AND CYTOGENETICS OF GONADAL AGENESIS. Am J Obstet Gynecol. 1963 Nov 1;87:578–600. doi: 10.1016/0002-9378(63)90051-6. [DOI] [PubMed] [Google Scholar]
- KLOTZ H. P., XIRAU J. [A recent case of "non-functioning ovaries"]. Sem Hop. 1962 Oct 14;38:3208–3210. [PubMed] [Google Scholar]
- LAMBERT A., NETTER A. [Male Turnerian pseudohermaphroditism]. Sem Hop. 1962 May 20;38:1699–1705. [PubMed] [Google Scholar]
- LEMLI L., SMITH D. W. THE XO SYNDROME. A STUDY OF THE DIFFERENTIATED PHENOTYPE IN 25 PATIENTS. J Pediatr. 1963 Oct;63:577–588. doi: 10.1016/s0022-3476(63)80368-6. [DOI] [PubMed] [Google Scholar]
- LINDSTEN J., FRACCARO M., POLANI P. E., HAMERTON J. L., SANGER R., RACE R. R. Evidence that the Xg blood group genes are on the short arm of the X chromosome. Nature. 1963 Feb 16;197:648–649. doi: 10.1038/197648a0. [DOI] [PubMed] [Google Scholar]
- LYON M. F. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature. 1961 Apr 22;190:372–373. doi: 10.1038/190372a0. [DOI] [PubMed] [Google Scholar]
- MELLMAN W. J., KLEVIT H. D., YAKOVAC W. C., MOORHEAD P. S., SAKSELA E. XO-XY CHROMOSOME MOSAICISM. J Clin Endocrinol Metab. 1963 Nov;23:1090–1095. doi: 10.1210/jcem-23-11-1090. [DOI] [PubMed] [Google Scholar]
- OIKAWA K., BLIZZARD R. M. Chromosomal studies of patients with congenital anomalies simulating those of gonadal aplasia, including a case of true gonadal and sex reversal. N Engl J Med. 1961 May 18;264:1009–1016. doi: 10.1056/NEJM196105182642001. [DOI] [PubMed] [Google Scholar]
- PARK W. W. The occurrence of sex chromatin in early human and macaque embryos. J Anat. 1957 Jul;91(3):369–373. [PMC free article] [PubMed] [Google Scholar]
- SHAH P. N., NAIK S. N., MAHAJAN D. K., DAVE M. J., PAYMASTER J. C. A new variant of human intersex with discussion on the developmental aspects. Br Med J. 1961 Aug 19;2(5250):474–477. doi: 10.1136/bmj.2.5250.474. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SOLOMON I. L., HAMM C. W., GREEN O. C. CHROMOSOME STUDIES ON TESTICULAR TISSUE CULTURES AND BLOOD LEUKOCYTES OF A MALE PREVIOUSLY REPORTED TO HAVE NO Y CHROMOSOME. N Engl J Med. 1964 Sep 17;271:586–592. doi: 10.1056/NEJM196409172711202. [DOI] [PubMed] [Google Scholar]
- TRITSCH H., SCHWARZ G. [Germinal aplasia and dwarfism]. Dtsch Med Wochenschr. 1963 Apr 5;88:701–passim. doi: 10.1055/s-0028-1111998. [DOI] [PubMed] [Google Scholar]
- TURNER H. H., GREENBLATT R. B., DOMINGUEZ H. Syndrome of gonadal dysgenesis and abdominal testis with an XO/XY chromosome mosaicism. J Clin Endocrinol Metab. 1963 Jul;23:709–716. doi: 10.1210/jcem-23-7-709. [DOI] [PubMed] [Google Scholar]
- TURPIN R., LEJEUNE J., LAFOURCADE J., CHIGOT P. L., SALMON C. [Presumption of monozygotism in spite of a sexual dimorphism: XY male subject and haploid X neuter subject]. C R Hebd Seances Acad Sci. 1961 May 8;252:2945–2946. [PubMed] [Google Scholar]
- WAXMAN S. H., GARTLER S. M., KELLEYVC Apparent masculinization of the female fetus diagnosed as true hermaphrodism by chromosomal studies. J Pediatr. 1962 Apr;60:540–544. doi: 10.1016/s0022-3476(62)80115-2. [DOI] [PubMed] [Google Scholar]
- WILLEMSE C. H. A patient suffering from Turner's syndrome and acromegaly. Acta Endocrinol (Copenh) 1962 Feb;39:204–212. doi: 10.1530/acta.0.0390204. [DOI] [PubMed] [Google Scholar]
- de GROUCHY, KLOTZ H. P., MASSIN J. P., CHIMENES H., NATHAN-KAHN J. [A recent case of XX/XO in a case of Turner's syndrome]. Sem Hop. 1962 Oct 14;38:3205–3208. [PubMed] [Google Scholar]