180 related articles for article (PubMed ID: 5517331)
1. [Tendency for chromosome breaks in Russel's syndrome].
Ganner E; Schwingshackl A
Klin Wochenschr; 1970 May; 48(10):629-32. PubMed ID: 5517331
[No Abstract] [Full Text] [Related]
2. [Familial Russell-syndrome (author's transl)].
Schwingshackl A; Ganner E; Hammerer I
Padiatr Padol; 1974; 9(2):130-7. PubMed ID: 4823694
[No Abstract] [Full Text] [Related]
3. Trisomy-18 mosaicism with features of Russel-Silver syndrome.
Chauvel PJ; Moore CM; Haslam RH
Dev Med Child Neurol; 1975 Apr; 17(2):220-4. PubMed ID: 1132609
[TBL] [Abstract][Full Text] [Related]
4. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
Hsia YE; Appadorai V; Breg WR; Howard RO
Birth Defects Orig Artic Ser; 1974; 10(8):19-25. PubMed ID: 4142400
[No Abstract] [Full Text] [Related]
5. [Monosomy of chromosome 21].
Rogóyski A; Babel M; Tronowska TD
Pediatr Pol; 1983 Jun; 58(6):557-9. PubMed ID: 6646915
[No Abstract] [Full Text] [Related]
6. [Trisomy 4p. A case presentation (author's transl)].
Delgado A; Egüés J; Muñoz M; González Villa P; Bernaola E; del Amo A
An Esp Pediatr; 1981 Oct; 15(4):383-9. PubMed ID: 7337304
[No Abstract] [Full Text] [Related]
7. IV. Application of the principles of genetic counseling.
Summitt RL
J Tenn Med Assoc; 1971 Apr; 64(4):323-32. PubMed ID: 5575761
[No Abstract] [Full Text] [Related]
8. 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]
9. [Pyknodysostosis. Review and report of 6 cases].
Nielsen EL
Ugeskr Laeger; 1973 Sep; 135(39):2093-8. PubMed ID: 4590079
[No Abstract] [Full Text] [Related]
10. Pycnodysostosis: a case report of a child with associated trisomy X.
Lacey SH; Eyring EJ; Shaffer TE
J Pediatr; 1970 Dec; 77(6):1033-8. PubMed ID: 5486620
[No Abstract] [Full Text] [Related]
11. [Identification of an unusual chromosome anomaly in a malformative syndrome].
Vianello MG; De Prà M
Minerva Pediatr; 1969 Apr; 21(15):611-8. PubMed ID: 5402255
[No Abstract] [Full Text] [Related]
12. [Spontaneous chromosomal instability in the rare hereditary diseases: Fanconi's anemia and Bloom's syndrome].
Schroeder TM
Dtsch Med Wochenschr; 1973 Nov; 98(46):2213-5. PubMed ID: 4757391
[No Abstract] [Full Text] [Related]
13. The genetics of thanatophoric dwarfism.
Pena SD; Goodman HO
Pediatrics; 1973 Jan; 51(1):104-9. PubMed ID: 4684427
[No Abstract] [Full Text] [Related]
14. Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosome.
Fryns JP; De Boeck K; Jaeken J; van den Berghe H
Hum Genet; 1978 Aug; 43(2):239-44. PubMed ID: 567620
[TBL] [Abstract][Full Text] [Related]
15. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
Murthy DS; Murthy SK; Banker GJ; Patel AJ
Indian Pediatr; 1991 May; 28(5):546-9. PubMed ID: 1684352
[No Abstract] [Full Text] [Related]
16. [Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].
Dutrillaux B; Laurent C; Robert JM; Lejeune J
Cytogenet Cell Genet; 1973; 12(4):245-53. PubMed ID: 4752866
[No Abstract] [Full Text] [Related]
17. [A genetic study of pycnodysostosis].
de Almeida LM
Ann Genet; 1972 Jun; 15(2):99-101. PubMed ID: 4537729
[No Abstract] [Full Text] [Related]
18. [Pyknodysostosis: report of 2 cases in the same family].
Reimão RN; Diament AJ
Arq Neuropsiquiatr; 1979 Dec; 37(4):412-9. PubMed ID: 533388
[No Abstract] [Full Text] [Related]
19. Autosomal syndromes.
Summitt RL
Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
[No Abstract] [Full Text] [Related]
20. [Ring chromosome 18. 18p-/18q- -deletion-syndrome].
Kunze J; Stephan E; Tolksdorf M
Humangenetik; 1972; 15(4):289-318. PubMed ID: 4565746
[No Abstract] [Full Text] [Related]
[Next] [New Search]