125 related articles for article (PubMed ID: 6965843)
1. Partial duplication of the long arm of chromosome 4.
Fryns JP; van den Berghe H
Ann Genet; 1980; 23(1):52-3. PubMed ID: 6965843
[TBL] [Abstract][Full Text] [Related]
2. Partial 4q duplication due to inherited der(20), t(4;20)(q25;q13)mat.
Sparkes RS; Francke U; Muller H; Toomey K
Ann Genet; 1977 Mar; 20(1):31-5. PubMed ID: 302670
[TBL] [Abstract][Full Text] [Related]
3. [Trisomy 4p. Mirror duplication of the short arm of chromosome 4 de novo].
Boyer JP; Andrieux L; Noel L; Mottet J
Neuropsychiatr Enfance Adolesc; 1983 Jul; 31(7):319-21. PubMed ID: 6621831
[No Abstract] [Full Text] [Related]
4. De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girl.
Jenkins EC; Curcuru-Giordano FM; Krishna SG; Cantarella J
Ann Genet; 1975 Jun; 18(2):117-20. PubMed ID: 1081364
[TBL] [Abstract][Full Text] [Related]
5. Partial distal 12q trisomy.
de Muelenaere A; Fryns JP; Van Den Berghe H
Ann Genet; 1980; 23(4):251-3. PubMed ID: 6971608
[TBL] [Abstract][Full Text] [Related]
6. Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome.
Fryns JP; Kleczkowska A; Decock P; Van den Berghe H
Ann Genet; 1990; 33(1):46-8. PubMed ID: 2195981
[TBL] [Abstract][Full Text] [Related]
7. Partial trisomy 15q: report of a patient and literature review.
Chandler K; Schrander-Stumpel CT; Engelen J; Theunissen P; Fryns JP
Genet Couns; 1997; 8(2):91-7. PubMed ID: 9219006
[TBL] [Abstract][Full Text] [Related]
8. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
San Martin V; Fernandez-Novoa C; Hevia A; Novales A; Fornell J; Galera H
Ann Genet; 1981; 24(4):248-50. PubMed ID: 6977308
[TBL] [Abstract][Full Text] [Related]
9. [Mental retardation in the crying cat syndrome. Comparison of the intellectual level in the partial deletion of the short arm of chromosome 5 with trisomy 21 and deletions of chromosome 18. Apropos of 118 cases taken from the literature].
Moor L
Rev Neuropsychiatr Infant; 1968 Mar; 16(3):257-67. PubMed ID: 5683042
[No Abstract] [Full Text] [Related]
10. [Neuropsychopathological aspects of 2 cases of 4p trisomy].
Giovannelli G; Pezzani C; Medioli Cavara F
Minerva Pediatr; 1974 Dec; 26(39):1933-43. PubMed ID: 4444708
[No Abstract] [Full Text] [Related]
11. Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation.
Engelen JJ; de Die-Smulders CE; Dirckx R; Verhoeven WM; Tuinier S; Curfs LM; Hamers AJ
Am J Med Genet; 2002 Apr; 109(2):149-53. PubMed ID: 11977164
[TBL] [Abstract][Full Text] [Related]
12. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
13. Inverted tandem ("mirror") duplications in human chromosomes: -nv dup 8p, 4q, 22q.
Taylor KM; Francke U; Brown MG; George DL; Kaufhold M
Am J Med Genet; 1977; 1(1):3-19. PubMed ID: 610424
[TBL] [Abstract][Full Text] [Related]
14. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
van Buggenhout G; Decock P; Fryns JP
Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
[TBL] [Abstract][Full Text] [Related]
15. Acne in retarded boy with autosomal chromosomal abnormality.
Funderburk SJ; Landau JW
Arch Dermatol; 1976 Jun; 112(6):859-61. PubMed ID: 133637
[TBL] [Abstract][Full Text] [Related]
16. de novo inversion-duplication of 2q35-2qter without growth retardation.
Dahoun-Hadorn S; Bretton-Chappuis B
Ann Genet; 1992; 35(1):55-7. PubMed ID: 1610122
[TBL] [Abstract][Full Text] [Related]
17. A case of nondisjunction of chromosome 21 (47,X,Yqs,+21) in an Indian family with Yqs.
Reddy KS; Thomas IM; Narayanan HS
Ann Genet; 1984; 27(3):194-6. PubMed ID: 6334487
[TBL] [Abstract][Full Text] [Related]
18. Supernumerary small chromosomal anomaly: report of three cases including one with a familial inversion of chromosome 5.
Lee Ml; Schneider J; Wasant P; Yu CY; Trpis L; Liang YW; Lewis BM; Borkowf S; Borgaonkar DS
J Genet Hum; 1978 Sep; 26(3):275-85. PubMed ID: 739263
[TBL] [Abstract][Full Text] [Related]
19. An extra small submetacentric chromosome: possible partial 18 trisomy.
Fujita K; Fujita HM
Jinrui Idengaku Zasshi; 1975 Mar; 19(4):371-5. PubMed ID: 1241595
[No Abstract] [Full Text] [Related]
20. [Partial trisomy for the long arm of chromosome 2 due to malsegregation of a maternal insertion : ins(6;2)(p22;q24q34)].
Couturier J; Aurias A; Prieur M; Barois A
Ann Genet; 1977 Mar; 20(1):52-5. PubMed ID: 302675
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]