238 related articles for article (PubMed ID: 7091195)
1. Duplication (5p13 leads to pter): prenatal diagnosis and review of the literature.
Khodr GS; Cadena G; Le KL; Kagan-Hallet KS
Am J Med Genet; 1982 May; 12(1):43-9. PubMed ID: 7091195
[TBL] [Abstract][Full Text] [Related]
2. [Prenatal diagnosis of the cri-du-chat syndrome in the case of balanced 5p--; 18p+ translocation in the mother].
Zolotukhina TV; Butomo IV; Rozovskiĭ IS; Grinberg KN
Genetika; 1981; 17(7):1304-8. PubMed ID: 7196856
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Cri du chat syndrome and translocation t(5p--;18p+).
Abrisqueta JA; Perez A; Aller V; Del Mazo J; Goday C; Martin MA; De Torres ML
J Genet Hum; 1976 Sep; 24(3):173-82. PubMed ID: 1003171
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
8. Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.
Sreekantaiah C; Kronn D; Marinescu RC; Goldin B; Overhauser J
Am J Med Genet; 1999 Sep; 86(3):264-8. PubMed ID: 10482877
[TBL] [Abstract][Full Text] [Related]
9. Dup(3)(p2----pter) in two families, including one infant with cyclopia.
Gimelli G; Cuoco C; Lituania M; Cordone M; Aricò M; Bianchi E; Maraschio P; Zuffardi O
Am J Med Genet; 1985 Feb; 20(2):341-8. PubMed ID: 3919583
[TBL] [Abstract][Full Text] [Related]
10. [Prenatal detection of crying cat syndrome due to balanced translocation in one parent].
Barjaktarović N; Pendić B; Garzicić B; Popovic M; Paljm A
Nouv Presse Med; 1977 Jan; 6(3):180-2. PubMed ID: 834552
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Prenatal diagnoses in a family with pericentric inversion of chromosome no. 5].
Körner H; Degen B; Röse I; Metschkarski S
Zentralbl Gynakol; 1983; 105(14):934-9. PubMed ID: 6624295
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Trisomy 5p: a report of 2 cases].
Alvarez-Coca J; García-Alix A; Delicado A; González M; Escribá R; López Pajares I; Morena V; Peralta A
An Esp Pediatr; 1985 Mar; 22(4):288-92. PubMed ID: 4003955
[TBL] [Abstract][Full Text] [Related]
15. [Familial segregation of a t(5p-;13q+). Complementary analysis from specimens preserved in liquid nitrogen].
Carpentier S; Dutrillaux B; Lafourcade J; Berger R; Rethoré MO; Lejeune J
Ann Genet; 1972 Mar; 15(1):57-60. PubMed ID: 4537617
[No 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. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13).
Coco R; del Rey G
J Genet Hum; 1978 Dec; 26(4):303-10. PubMed ID: 752064
[TBL] [Abstract][Full Text] [Related]
18. The "cri du chat" syndrome.
Mladkovskaya TB; Lebedev BV; Mazaeva IV
Sov Genet; 1970 Oct; 6(10):1374-9. PubMed ID: 4272596
[No Abstract] [Full Text] [Related]
19. 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]
20. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.
Verma RS; Dosik H; Wexler IB
J Genet Hum; 1977 Dec; 25(4):295-301. PubMed ID: 599332
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
