178 related articles for article (PubMed ID: 5313392)
1. Clinical, cytogeneti and autoradiographic studies in 0 cases with rare chromosome disorders. IV. Cases 9 and 10.
Moore MK; Engel E
Ann Genet; 1970 Dec; 13(4):269-74. PubMed ID: 5313392
[No Abstract] [Full Text] [Related]
2. 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]
3. [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)].
Lejeune J; Berger R; Réthoré MO; Lafourcade J; Dutrillaux B; Canlorbe P; Labrune B
Ann Genet; 1967 Mar; 10(1):18-24. PubMed ID: 5300122
[No Abstract] [Full Text] [Related]
4. [The "Copenhagen chromosome" (syndrome of the small metacentric extra-chromosome)].
Haberlandt W
Arztl Forsch; 1971 Jul; 25(7):218-23. PubMed ID: 5109598
[No Abstract] [Full Text] [Related]
5. [Autosomal chromosome aberrations].
Serville F; Battin J
Bord Med; 1971 May; 4(5):1373-416. PubMed ID: 5105683
[No Abstract] [Full Text] [Related]
6. [Cytogenetic survey in 105 psychiatric hospital patients].
Bourgeois M; Benezech M; Limousin G
Ann Med Psychol (Paris); 1974 Dec; 2(5):734-43. PubMed ID: 4458595
[No Abstract] [Full Text] [Related]
7. Clinical, cytogenetic and autoradiographic studies in 10 cases with rare chromosome disorders II. Cases 3,4 and 5.
Moore MK; Engel E
Ann Genet; 1970 Jun; 13(2):129-34. PubMed ID: 5310697
[No Abstract] [Full Text] [Related]
8. The 18p- syndrome. Report of two cases.
Jacobsen P; Mikkelsen M
Ann Genet; 1968 Dec; 11(4):211-6. PubMed ID: 5306362
[No Abstract] [Full Text] [Related]
9. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
[No Abstract] [Full Text] [Related]
10. Familial transmission of a Gq- (Ph1-like) chromosome.
Ricci N; Dallapiccola B; Preto G
Ann Genet; 1970 Dec; 13(4):263-4. PubMed ID: 5313390
[No Abstract] [Full Text] [Related]
11. Clinical, cytogenetic and autoradiographic studies in 10 cases with rare chromosome disorders. 3. Cases 6, 7 and 8.
Moore MK; Engel E
Ann Genet; 1970 Sep; 13(3):207-12. PubMed ID: 5313151
[No Abstract] [Full Text] [Related]
12. [Ring chromosome 22. Description of a new case (1)].
Gil Benso R; López Ginés C; Gregori Romero M; Galán Sánchez F; Pellín Pérez A
An Esp Pediatr; 1991 Jul; 35(1):62-4. PubMed ID: 1772175
[No Abstract] [Full Text] [Related]
13. Mosaic isochromosome 8p.
Tilstra DJ; Grove M; Spencer AC; Norwood TH; Pagon RA
Am J Med Genet; 1993 Jun; 46(5):517-9. PubMed ID: 8322812
[TBL] [Abstract][Full Text] [Related]
14. [A new case of a ring shaped chromosome 18 (18 r)].
Petit P; Poncelet R
Ann Genet; 1967 Sep; 10(3):134-7. PubMed ID: 5300397
[No Abstract] [Full Text] [Related]
15. [Ring chromosomes in mosaicism 46, XY, Cr-46, XY].
Ferrier S; Freund M; Grétillat A
Arch Genet (Zur); 1973; 46(1):1-14. PubMed ID: 4731928
[No Abstract] [Full Text] [Related]
16. De novo partial monosomy 21 with unusual karyotype.
Al-Awadi SA; Naguib KK; Teebi AS; Sundareshan TS
Jinrui Idengaku Zasshi; 1986 Mar; 31(1):45-8. PubMed ID: 3735757
[No Abstract] [Full Text] [Related]
17. Asymmetric clinical and cytogenetic findings in a 4-year-old girl with trisomy 18 mosaicism.
Rao KW; Buchanan PD; Aylsworth AS
Birth Defects Orig Artic Ser; 1978; 14(6C):349-54. PubMed ID: 728589
[No Abstract] [Full Text] [Related]
18. Mosaic supernumerary small ring chromosome.
Fryns JP; van Herck G; van den Berghe H
J Genet Hum; 1981 Jun; 29(2):151-4. PubMed ID: 7328409
[No Abstract] [Full Text] [Related]
19. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".
Curry CJ; Ying KL; O'Lague P; Tsai J
Birth Defects Orig Artic Ser; 1982; 18(3B):275-86. PubMed ID: 7139110
[No Abstract] [Full Text] [Related]
20. [A case of translocation t(Cp-; Bp+)].
Ricci N; Ventimiglia B; Dallapiccola B; Preto G
Ann Genet; 1967 Jun; 10(2):82-5. PubMed ID: 5298977
[No Abstract] [Full Text] [Related]
[Next] [New Search]
