Chromosomal Abnormalities and Oral Anomalies

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Lennox, B. Chromosomes for Beginners, Lancet, 1 :1046-50, 1961.

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Hungerford, D.A. , et al. The Chromosome Constitution of a Human Phenotypic Intersex, Amer. J. hum. Genet., 11:215-36, 1959.

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Böök, J.A. , et al. Cytogenetical Observations in Mongolism , Acta paediat., 48:453-68, 1959.

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Ford, C.E. , et al. The Chromosomes in a Patient Showing Both Mongolism and the Klinefelter Syndrome, Lancet, 1:709-10, 1959.

Brown, R.H. , and Cunningham, W.M. Some Dental Manifestations of Mongolism , Oral Surg., 14:664-76, 1961.

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Levinson, A. , et al. Variability of Mongolism, Pediatrics, 16:43-54, 1955.

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Thomson, J. Note on the Peculiarities of the Tongue in Mongolism and on Tongue Sucking in Their Causation, Brit. med. J., 1:1051, 1907.

Magri, E. Contributo allo studio dei caratteri dentl-maxillo-facciale nel mongolismo , Acta stomat. (Padua), 2:119-28, 1955.

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Polani, P.E. , et al. Mongol Girl with 46 Chromosomes, Lancet, 1 :721-24, 1960.

Spitzer, R. A Case of Mongolism, Brit. dent. J., 103:249, 1957.

Cohen, M.M. , Winer, R.A. , Schwartz, S. , and Shklar, G. Oral Aspects of Mongolism. I. Periodontal Disease in Mongolism, Oral Surg., 14:92-107, 1961.

Dow, R.S. A Preliminary Study of Periodontoclasia in Mongolian Children at Polk State School, Amer. J. ment. Defic. , 55:535-38, 1951.

Hjorting-Hansen, E. , et al. Orale Manifestationer ved Macroglobulinemia Waldenstrom, Ugeskr. Lœg., in press.

Crawfurd, M. d'A. Multiple Congenital Anomaly Associated with an Extra Chromosome, Lancet, 2:22-24, 1961.

Edwards, J.H. , et al. New Trisomic Syndrome, Lancet, 1:787-90, 1960.

Smith, E.W. , et al. A New Autosomal Trisomy Syndrome: Multiple Congenital Anomalies Caused by an Extra Chromosome. J. Pedial., 57:338-45, 1960.

Uchida, I.A. , and Bowman, J.M. XXX-18 Trisomy, Lancet, 2:1094, 1961.

Ellis, J.R. , and Marwood, J.C. Autosomal Trisomy Syndromes, Lancet, 2:211-12, 1961.

Patau, K. , et al. Multiple Congenital Anomaly Caused by an Extra Autosome, Lancet, 2:790-93, 1960.

Van Wijck, J.A.M. , et al. Trisomic Child of Hyperthyroid Mother, Lancet, 1 :877, 1961.

Atkins, L. , and Rosenthal, M.K. Multiple Congenital Anomalies Associated with Chromosomal Trisomy, New Engl . J. Med., 265:314-18, 1961.

Lubs, H.A., JR. , et al. Trisomy 13-15-a Clinical Syndrome, Lancet, 2:1001-2, 1961.

McEvery, E.T. , and Brennemann , J. Multiple Facial Anomalies , J. Pediat., 11 :468-74, 1937.

Therman, E. , et al. The D Trisomy Syndrome and XO Gonadal Dysgenesis in Two Sisters, Amer. J. hum. Genet., 13:193-204, 1961.

Turner, H.H. A Syndrome of Infantilism, Congenital Webbed Neck, Cubitus Valgus, Endocrinology, 23 :566-74, 1938.

Oberman, J.W. The Prepuberal Diagnosis of Ovarian Agenesis and Its Relationship to Status Bonnevie-Ullrich, J. Pediat. , 47:48-59, 1955.

Ford, C.E. , et al. A Sex Chromosomal Anomaly in a Case of Gonadal Dysgenesis (Turner's Syndrome), Lancet, 1:711-13, 1959.

Vaharu, T. Gonadal Dysplasia and Enlarged Phallus in a Girl with 45 Chromosomes plus "Fragment," Lancet, 1:1351, 1961.

Grumbach, M.M. , et al. Chromosomal Sex in Gonadal Dysgenesis (Ovarian Agenesis), J. clin. Endocr., 15:1161-93, 1955.

Jackson, W.P.U. , and Sougin-Mibashan , R. Turner's Syndrome in the Female, Brit. med. J., 2 :368-71, 1953.

Wade, W.G. , et al. A Case of Gonadal Dysgenesis or the Ullrich-Turner Syndrome with Androgenic Manifestations, Arch. Dis. Child., 31:354-57, 1956.

Wilkins, L. , and Fleischmann , W. Ovarian Agenesis, J. clin. Endocr., 4:357-75, 1944.

Costillo, E.B. , et al. Syndrome of Rudimentary Ovaries with Estrogen Insufficiency and Increase in Gonadotropins, J. Clin. Endocr., 7:385-93, 1947.

Silver, H.K. , and Dodd, S.G. Gonadal Dysgenesis. Bonnevie-Ullrich-Turner Syndrome with Elevated Urinary Gonadotropins in a Nine Year Old Child, Amer. J. Dis. Child., 94:702-7, 1957.

Turner, E.K. A Case of Probable Ovarian Agenesis with Turner Syndrome in a Female Child Aged Seven Months, Med. J. Aust. , 1:39-42, 1954.

Silver, H.K. , and Kempe, C.H. Ovarian Agenesis (Congenital Aplastic Ovaries) in Child, Amer. J. Dis. Child., 85:523-30, 1953.

Schneider, R.W. , and Mccullagh , E.P. Infantilism, Congenital Webbed Neck and Cubitus Valgus (Turner's Syndrome), Cleveland Clin. Quart., 10 :112-25, 1943.

Klinefelter, H.F., JR. , et al. Syndrome Characterized by Gynecomastia, Aspermatogenesis without A-Leydigism and Increased Excretion of Follicle-stimulating Hormone, J. clin. Endocr., 2:615-27, 1942.

Jacobs, P.A. , and Strong, J.A. A Case of Human Intersexuility Having a Possible XXV Sex Determining Mechanism, Nature, 183:302-3, 1959.

Mosier, H.D. , et al. The Frequency of the Positive Sex Chromatin Pattern in Males with Mental Deficiency, Pediatrics, 25:291-97, 1960.

Stewart, J.S.S. Klinefelter's Syndrome, Clinical and Hormonal Aspects, Quart. J. Med., 28: 561-72, 1959.

--. Medullary Gonadal Dysgenesis ( Chromatin Positive Klinefelter's Syndrome) , Lancet, 1:1176-78,1959.

Mosier, H.D. , et al. Sexually Deviant Behavior in Klinefelter's Syndrome, J. Pediat., 57:479-83, 1960.

Balze, F.A. De LA , et al. Klinefelter's Syndrome, J. clin. Endocr., 12:1426-44, 1952.

Carr, D.H. , et al. An XXXY Sex Chromosomal Complex in Klinefelter Subjects with Duplicate Sex Chromatin, J. Clin. Endocr., 21:491-505, 1961.

--. A Probable XXYY Sex Determining Mechanism in a Mentally Deficient Male with Klinefelter's Syndrome, Canad. med. Ass. J., 84:873-78, 1961.

Ferguson-Smith, M.A. , et al. Primary Amentia and Microorchidism Associated with an XXXY Sex Chromosome Constitution, Lancet , 2:184-87, 1960.

Miller, O.J. , et al. A Family with an XXXXY Male, a Leukemic Male and Two 21-Trisomic Mongoloid Females, Lancet, 2:78-79, 1961.

Fraser, J.H. , et al. A Case of XXXXY Klinefelter's Syndrome , Lancet , 2:1064-67, 1961.

Miller, O.J. , et al. A Family with an XXXY Male, a Leukemic Male and Two 21-Trisomic Mongoloid Females, Lancet, 1:78-79, 1961.

Ellis, J.R. , et al. A Male with XXYY Chromosomes, Ann. Hum. Genet., 25:145-52, 1961.

Carr, D.H. , et al. A Probable XXYY Sex Determining Mechanism in a Mentally Defective Male with Klinefelter Syndrome, Canad. Med. Ass. J., 84:873-78, 1961.

Jacobs, P.A. , Baikie, A.G. , Brown , W.M. , Macgregor, T.N. , Maclean, N. , and Harnden, D.G. Evidence for the Existence of the Human "Super Female," Lancet, 2:423-25, 1959.

Fraser, J.H. , et al. The XXX Syndrome Frequency among Mental Defectives and Fertility, Lancet, 2:626-27, 1960.

Jacobs, P.A. , et al. Abnormalities Involving the X Chromosome in Women, Lancet, 1:1213-16, 1960.

Stewart, J.S.S. , and Sanderson, A.R. Fertility and Oligophrenia in an Apparent Triple-X Female, Lancet, 2:21-23, 1960.

Decarli, L. , et al. Trisomic Condition of a Large Chromosome in a Woman with Mongoloid Traits, Lancet, 2:130-31, 1960.

Sandberg, A.A. , Crosswhite, L.H. , and Gordy, E. Trisomy for a Large Chromosome, J. Amer. med. Ass., 174:221-25, 1960.

Turner, B. , and Jennings, A.N. Trisomy for Chromosome 22, Lancet, 22:49-50, 1961.

Dunn, H.G. , et al. Benign Congenital Hypotonia with Chromosomal Anomaly, Pediatrics, 28: 578-91, 1961.

Sandberg, A.A. An XYY Human Male, Lancet, 2:488-89,1961.

Böök, J.A. , and Santesson, B. Malformation Syndrome in Man Associated with Triploidy (69 Chromosomes), Lancet, 1:858-59, 1960.

Delhanty, J.D.A. , et al. Triploid Cells in a Human Embryo, Lancet, 1 :1286, 1961.

Pemrose, L.S. , and Delhanty, J.D.A. Triploid Cell Cultures from a Macerated Fetus, Lancet, 1 :1261-62, 1961.