771 related articles for article (PubMed ID: 3960564)
1. Cri du chat-syndrome in combination with partial trisomy 9 p.
Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD
Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564
[TBL] [Abstract][Full Text] [Related]
2. Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect.
Petit P; Fryns JP
Genet Couns; 1990; 1(2):179-84. PubMed ID: 2081002
[TBL] [Abstract][Full Text] [Related]
3. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
[TBL] [Abstract][Full Text] [Related]
4. Variability in a family with an insertion involving 5p.
Marinescu RC; Mamunes P; Kline AD; Schmidt J; Rojas K; Overhauser J
Am J Med Genet; 1999 Sep; 86(3):258-63. PubMed ID: 10482876
[TBL] [Abstract][Full Text] [Related]
5. [Partial monosomy and trisomy 5 p due to balanced translocation t (3,5) in the father (author's transl)].
Andrle M; Erlach A; Rett A
Wien Klin Wochenschr; 1981 Jan; 93(1):16-9. PubMed ID: 7222705
[TBL] [Abstract][Full Text] [Related]
6. Duplication 11q and deletion 5p syndromes due to a reciprocal translocation segregating in four generations.
Mutchinick O; Ramos Z; Sánchez F; Ruz L; Lisker R; Ovseyevitz J
Am J Med Genet; 1988 Jan; 29(1):187-92. PubMed ID: 3344767
[TBL] [Abstract][Full Text] [Related]
7. [A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
Hu JC; Tan K; Cheng DH; Li LY; Lu GX; Tan YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):87-90. PubMed ID: 23450488
[TBL] [Abstract][Full Text] [Related]
8. [Cri-du-chat syndrome and trisomy 8p due to a paternal translocation t(5;8)(p1409;p12)].
Rethoré MO; Couturier J; Villain E; Hambourg M; Lejeune J
Ann Genet; 1984; 27(2):118-21. PubMed ID: 6331789
[TBL] [Abstract][Full Text] [Related]
9. [Autosome syndromes].
Boczkowski K
Pol Tyg Lek; 1983 Sep; 38(38):1191-4. PubMed ID: 6369277
[No Abstract] [Full Text] [Related]
10. Cytogenetics and the pathologist.
Carr DH
Pathol Annu; 1975; 10():93-144. PubMed ID: 126409
[No Abstract] [Full Text] [Related]
11. Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocation.
Leisti J; Kaback MM; Rimoin DL
Birth Defects Orig Artic Ser; 1975; 11(5):317-9. PubMed ID: 1218232
[No Abstract] [Full Text] [Related]
12. Cri du chat syndrome [46, XY, 5p-] with balanced B/F translocation in father and grandfather: a case report.
Char F
Birth Defects Orig Artic Ser; 1974; 10(10):49-53. PubMed ID: 4462641
[No Abstract] [Full Text] [Related]
13. Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation.
Gencik A; Gencikova A; Pálova A
Acta Paediatr Acad Sci Hung; 1982; 23(3):291-8. PubMed ID: 7180435
[TBL] [Abstract][Full Text] [Related]
14. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
Murru D; Boccone L; Ristaldi MS; Nucaro AL
Genet Couns; 2008; 19(4):381-6. PubMed ID: 19239081
[TBL] [Abstract][Full Text] [Related]
15. De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation.
Chaganti RS; Morillo-Cucci G; Friis L; Degnan M; German J
Ann Genet; 1976 Mar; 19(1):43-8. PubMed ID: 1084121
[TBL] [Abstract][Full Text] [Related]
16. [Identification of 2 familial translocations].
Laurent C; Biemont MC; Robert JM; Dutrillaux B
Ann Genet; 1974 Dec; 17(4):279-81. PubMed ID: 4548825
[No Abstract] [Full Text] [Related]
17. A 45,XX,-5,-14,+t(5q;14q)mat cri du chat child.
Bass HN; Sparkes RS; Crandall BF; Galos KJ; Howard J
Ann Genet; 1978 Mar; 21(1):56-9. PubMed ID: 308345
[TBL] [Abstract][Full Text] [Related]
18. Clinical delineation of a patient with trisomy 1q32.qter and monosomy 5p resulting from a familial translocation 1;5.
Flores Ramírez F; Abreu González M; García Delgado C; Aparicio Onofre A; Guevara Yáñez R; Sánchez Urbina R; Murguía Peniche T; Ramírez-Ortíz MA; Ibarra Ríos D; Ortiz de Luna RI; Cervantes Peredo AB; Morán Barroso VF
Genet Couns; 2010; 21(4):363-73. PubMed ID: 21290965
[TBL] [Abstract][Full Text] [Related]
19. [The chromosomal syndromes (author's transl)].
Klein D
Padiatr Padol Suppl; 1975; 4():1-31. PubMed ID: 127145
[TBL] [Abstract][Full Text] [Related]
20. [The intelligence level in the chromosome aberrations affecting autosomes].
Moor L
Rev Neuropsychiatr Infant; 1970 Dec; 18(12):943-66. PubMed ID: 4251821
[No Abstract] [Full Text] [Related]
[Next] [New Search]