451 related articles for article (PubMed ID: 8135287)
1. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
Qumsiyeh MB; Stevens CA
Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
[TBL] [Abstract][Full Text] [Related]
2. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
Syrrou M; Borghgraef M; Fryns JP
Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
[TBL] [Abstract][Full Text] [Related]
3. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
Cai T; Yu P; Tagle DA; Xia J
Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
[TBL] [Abstract][Full Text] [Related]
4. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F
J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
[TBL] [Abstract][Full Text] [Related]
5. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
6. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.
Wheeler PG; Weaver DD; Palmer CG
Am J Med Genet; 1995 Feb; 55(4):462-5. PubMed ID: 7762587
[TBL] [Abstract][Full Text] [Related]
7. Characterization of a derivative chromosome 17 by fish-technique.
Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
[TBL] [Abstract][Full Text] [Related]
8. On the deletion 4p16 Wolf-Hirschhorn syndrome.
Rivas F; Hernandez A; Nazara Z; Fragoso R; Olivares N; Rolon A; Cantu JM
Ann Genet; 1979; 22(4):228-31. PubMed ID: 317787
[TBL] [Abstract][Full Text] [Related]
9. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
Harvard C; Malenfant P; Koochek M; Creighton S; Mickelson EC; Holden JJ; Lewis ME; Rajcan-Separovic E
Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocation.
Bauer K; Howard-Peebles PN; Keele D; Friedman JM
Am J Med Genet; 1985 Jun; 21(2):351-6. PubMed ID: 4014316
[TBL] [Abstract][Full Text] [Related]
12. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.
Harrison KJ; Teshima IE; Silver MM; Jay V; Unger S; Robinson WP; James A; Levin A; Chitayat D
Am J Med Genet; 1998 Sep; 79(2):103-7. PubMed ID: 9741467
[TBL] [Abstract][Full Text] [Related]
13. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
Cetin Z; Mihci E; Keser I; Karaali K; Berker S; Luleci G
Genet Couns; 2012; 23(2):239-47. PubMed ID: 22876583
[TBL] [Abstract][Full Text] [Related]
14. Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.
Estabrooks LL; Rao KW; Korf B
Am J Med Genet; 1993 Jan; 45(1):97-100. PubMed ID: 8418669
[TBL] [Abstract][Full Text] [Related]
15. A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.
Goodship J; Curtis A; Cross I; Brown J; Emslie J; Wolstenholme J; Bhattacharya S; Burn J
J Med Genet; 1992 Jul; 29(7):451-4. PubMed ID: 1640422
[TBL] [Abstract][Full Text] [Related]
16. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
[TBL] [Abstract][Full Text] [Related]
17. "Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.
Zollino M; Wright TJ; Di Stefano C; Tosolini A; Battaglia A; Altherr MR; Neri G
Am J Med Genet; 1999 Feb; 82(5):371-5. PubMed ID: 10069706
[TBL] [Abstract][Full Text] [Related]
18. 10p duplication characterized by fluorescence in situ hybridization.
Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems.
Laczmanska I; Stembalska A; Gil J; Czemarmazowicz H; Sasiadek M
Eur J Med Genet; 2006; 49(1):87-92. PubMed ID: 16473315
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
