214 related articles for article (PubMed ID: 4124236)
1. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
Rethoré MO; Hoehn H; Rott HD; Couturier J; Dutrillaux B; Lejeune J
Humangenetik; 1973 Apr; 18(2):129-38. PubMed ID: 4124236
[No Abstract] [Full Text] [Related]
2. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
Sanchez O; Yunis JJ; Escobar JI
Humangenetik; 1974 Apr; 22(1):59-65. PubMed ID: 4134840
[No Abstract] [Full Text] [Related]
3. Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.
Podruch PE; Weisskopf B
J Pediatr; 1974 Jul; 85(1):92-5. PubMed ID: 4855265
[No Abstract] [Full Text] [Related]
4. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
[No Abstract] [Full Text] [Related]
5. Malformative syndrome with ring chromosome 13.
Fryns JP; Deoover J; Van den Berghe H
Humangenetik; 1974; 24(3):235-40. PubMed ID: 4140834
[No Abstract] [Full Text] [Related]
6. Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23).
Kroyer S; Niebuhr E
Ann Genet; 1975 Mar; 18(1):50-5. PubMed ID: 50043
[TBL] [Abstract][Full Text] [Related]
7. Mosaic-trisomy and pericentric inversion of chromosome 9 in a malformed boy.
Schinzel A; Hayashi K; Schmid W
Humangenetik; 1974; 25(3):171-7. PubMed ID: 4141334
[No Abstract] [Full Text] [Related]
8. Partial trisomy 8: trisomy of the distal part of the long arm of chromosome number 8 plus (8q2) in a severely retarded and malformed girl.
Fryns JP; Verresen H; Van den Berghe H
Humangenetik; 1974; 24(3):241-6. PubMed ID: 4140835
[No Abstract] [Full Text] [Related]
9. Partial trisomy 9 in the case of familial translocation 8/9 mat.
Schwanitz G; Schamberger U; Rott HD; Wieczorek V
Ann Genet; 1974 Sep; 17(3):163-6. PubMed ID: 4548816
[No Abstract] [Full Text] [Related]
10. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
Raoul O; Rethoré MO; Dutriliaux B; Michon L; Lejeune J
Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
[TBL] [Abstract][Full Text] [Related]
11. A case of a girl with a 21 ring chromosome.
Kucerová M; Polívková Z
Hum Hered; 1974; 24(1):100-4. PubMed ID: 4136482
[No Abstract] [Full Text] [Related]
12. Trisomy for the distal half of the short arm of chromosome 9. A variant of the trisomy 9p syndrome.
Lewandowski RC; Yunis JJ; Lehrke R; O'Leary J; Swaiman KF; Sanchez O
Am J Dis Child; 1976 Jun; 130(6):663-7. PubMed ID: 937286
[TBL] [Abstract][Full Text] [Related]
13. An extra small metacentric chromosome in a mentally retarded boy.
Ishmael J; Laurence KM
J Med Genet; 1968 Dec; 5(4):335-40. PubMed ID: 5713650
[No Abstract] [Full Text] [Related]
14. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
Miller JQ
Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
[No Abstract] [Full Text] [Related]
15. [Trisomy 9p gy t(4; 9) (q 34; q21) mat].
Rethoré MO; Ferrand J; Dutrillaux B; Lejeune J
Ann Genet; 1974 Sep; 17(3):157-61. PubMed ID: 4548815
[No Abstract] [Full Text] [Related]
16. Familial C-G translocation in three relatives associated with severe mental retardation, short stature, unusual dermatoglyphics and other malformations.
Yanagisawa S; Hiraoka K
J Ment Defic Res; 1971 Jun; 15(2):136-46. PubMed ID: 5559234
[No Abstract] [Full Text] [Related]
17. Translocation, t(4qminus;13qplus), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation.
Schrott HG; Sakaguchi S; Francke U; Luzzatti L; Fialkow PJ
J Med Genet; 1974 Jun; 11(2):201-5. PubMed ID: 4135220
[TBL] [Abstract][Full Text] [Related]
18. 9p trisomy identified by Giemsa-11.
Wyandt HE; Hecht F; Magenis RE; Wysham DG; Prescott G
Hum Genet; 1976 Mar; 31(3):355-8. PubMed ID: 955631
[TBL] [Abstract][Full Text] [Related]
19. Brother and sister with trisomy 10p: a new syndrome.
Schleiermacher E; Schliebitz U; Steffens C
Humangenetik; 1974; 23(3):163-72. PubMed ID: 4844639
[No Abstract] [Full Text] [Related]
20. Trisomy 9p with an isochromosome of 9p.
Smith G; McCaa A; Kelly TE
Hum Genet; 1978 May; 42(1):93-7. PubMed ID: 649175
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]