222 related articles for article (PubMed ID: 5096548)
41. [Mental retardation and sexual development in chromosomal syndrome (author's transl)].
Balestrazzi P; Bernasconi S; Medioli FC; Corrini L; Villani G
Ateneo Parmense Acta Biomed; 1980; 51(1):45-51. PubMed ID: 7470180
[TBL] [Abstract][Full Text] [Related]
42. Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.
Fischer P; Golob E; Friedrich F; Kunze-Mühl E; Doleschel W; Aichmair H
J Med Genet; 1970 Mar; 7(1):91-8. PubMed ID: 5480972
[No Abstract] [Full Text] [Related]
43. Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion.
Funderburk SJ; Crandall BF
Am J Hum Genet; 1974 Nov; 26(6):715-22. PubMed ID: 4140688
[No Abstract] [Full Text] [Related]
44. Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
Wyandt HE; Hecht F; Lovrien EW; Stewart RE
Cytogenetics; 1971; 10(6):413-26. PubMed ID: 5146418
[No Abstract] [Full Text] [Related]
45. E ring chromosome with persistent left superior vena cava and hypertrophic subaortic stenosis.
Wald S; Engel E; Nance WE; Davies J; Puyau FA; Sinclair-Smith BC
J Med Genet; 1969 Sep; 6(3):328-33. PubMed ID: 5388064
[No Abstract] [Full Text] [Related]
46. The cytological behavior of a human ring-chromosome.
Gripenberg U
Chromosoma; 1967; 20(3):284-9. PubMed ID: 5619940
[No Abstract] [Full Text] [Related]
47. [Developmental anomalies in children with a ring chromosome in group E].
Sokolowski J; Baniowski A; Stopyrowa J; Kleczkowska A; Kubień E
Pediatr Pol; 1970 Nov; 45(11):1341-50. PubMed ID: 4322155
[No Abstract] [Full Text] [Related]
48. [The autosomal chromosome aberrations in ophthalmology].
François J
J Genet Hum; 1966; 15():Suppl:133-208. PubMed ID: 4873685
[No Abstract] [Full Text] [Related]
49. Cytogenetic study of individuals suspected of chromosome anomalies.
Singh DN
Clin Pediatr (Phila); 1977 Jul; 16(7):619-22. PubMed ID: 862299
[No Abstract] [Full Text] [Related]
50. [A new observation of a ring chromosome 18].
Deminatti M; Dupuis C; Maillard E; Delmas-Marsalet Y; Bulteel MF
Ann Genet; 1969 Jun; 12(2):126-9. PubMed ID: 5308385
[No Abstract] [Full Text] [Related]
51. B-F chromosome translocation associated with father-child incompatibility within the Gc-system.
Henningsen K; Jacobsen P; Mikkelsen M
Hum Hered; 1969; 19(3):283-7. PubMed ID: 5361492
[No Abstract] [Full Text] [Related]
52. Gene deletion and duplication effects on phenotype and gamma globulin levels.
Rudd NL; Lamarche PH
J Med Genet; 1971 Mar; 8(1):97-106. PubMed ID: 5098075
[No Abstract] [Full Text] [Related]
53. The "cri du chat" syndrome.
Mladkovskaya TB; Lebedev BV; Mazaeva IV
Sov Genet; 1970 Oct; 6(10):1374-9. PubMed ID: 4272596
[No Abstract] [Full Text] [Related]
54. Tetraploidy and 18-trisomy in a six-year-old triple mosaic boy.
Atnip RL; Summitt RL
Cytogenetics; 1971; 10(5):305-17. PubMed ID: 5156365
[No Abstract] [Full Text] [Related]
55. Ring chromosome 16.
Neidengard L; Sparkes RS
Hum Genet; 1981; 59(2):175-7. PubMed ID: 7327577
[No Abstract] [Full Text] [Related]
56. A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.
Valdmanis A; Pearson G; Siegel AE; Hoeksema RH; Mann JD
Ann Genet; 1967 Dec; 10(4):159-66. PubMed ID: 5301688
[No Abstract] [Full Text] [Related]
57. Structural variation in human nitotic chromosomes.
Leisti J
Ann Acad Sci Fenn Biol; 1971; 179():1-69. PubMed ID: 4261167
[No Abstract] [Full Text] [Related]
58. Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18.
Fraccaro M; Herin P; Hultén M; Ivemark BI; Jonasson J; Lindsten J; Tiepolo L; Zetterqvist P
Ann Genet; 1972 Jun; 15(2):93-8. PubMed ID: 4537728
[No Abstract] [Full Text] [Related]
59. A retarded child with a 46XX,3p-q+ chromosome karyotype.
Butler LJ; Hall ME; Wharton BA
J Ment Defic Res; 1974 Mar; 18(0):41-9. PubMed ID: 4424443
[No Abstract] [Full Text] [Related]
60. A case of 18q- in a t(18q-;6p+) family.
Jacobsen P; Mikkelsen M; Niebuhr E; de Grouchy J
Ann Genet; 1971 Mar; 14(1):41-8. PubMed ID: 5314293
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
