157 related articles for article (PubMed ID: 3344775)
1. A case of ring (9)/del(9p) mosaicism associated with gastroesophageal reflux.
Leung AK; Rudd NL
Am J Med Genet; 1988 Jan; 29(1):43-8. PubMed ID: 3344775
[TBL] [Abstract][Full Text] [Related]
2. Another case of ring chromosome 9 associated with gastroesophageal reflux.
Manouvrier-Hanu S; Turck D; Farriaux JP
Am J Med Genet; 1989 Apr; 32(4):558. PubMed ID: 2774007
[No Abstract] [Full Text] [Related]
3. Metacarpophalangeal pattern profile analysis in a patient with ring (9)/del(9p) mosaicism.
Leung AK; McLeod DR; Nudd NL
Am J Med Genet; 1988 Oct; 31(2):481-2. PubMed ID: 3232712
[No Abstract] [Full Text] [Related]
4. Two forms of ring 13 in a child with rhabdomyosarcoma.
Voullaire LE; Petrovic V; Sheffield LJ; Campbell P
Am J Med Genet; 1991 Jun; 39(3):285-7. PubMed ID: 1867278
[TBL] [Abstract][Full Text] [Related]
5. Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s.
Wenger SL; Boone LY; Cummins JH; Del Vecchio MA; Bay CA; Hummel M; Mowery-Rushton PA
Am J Med Genet; 2000 Apr; 91(5):351-4. PubMed ID: 10766997
[TBL] [Abstract][Full Text] [Related]
6. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
[TBL] [Abstract][Full Text] [Related]
7. Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son.
Fryns JP; Kleczkowska A; Smeets E; Van Den Berghe H
Ann Genet; 1992; 35(2):121-3. PubMed ID: 1524410
[TBL] [Abstract][Full Text] [Related]
8. Mosaic r(13) in an infant with aprosencephaly.
Goldsmith CL; Tawagi GF; Carpenter BF; Speevak MD; Hunter AG
Am J Med Genet; 1993 Sep; 47(4):531-3. PubMed ID: 8256818
[TBL] [Abstract][Full Text] [Related]
9. Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome.
Juyal RC; Kuwano A; Kondo I; Zara F; Baldini A; Patel PI
Am J Med Genet; 1996 Dec; 66(2):193-6. PubMed ID: 8958329
[TBL] [Abstract][Full Text] [Related]
10. Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation.
Frizzley JK; Stephan MJ; Lamb AN; Jonas PP; Hinson RM; Moffitt DR; Shkolny DL; McDermid HE
J Med Genet; 1999 Mar; 36(3):237-41. PubMed ID: 10204853
[TBL] [Abstract][Full Text] [Related]
11. Multiple critical smallest region of overlap in monosomy 16Q syndrome?
Doco-Fenzy M; Elchardus JF; Brami G; Digeon B; Gruson N; Adnet JJ
Genet Couns; 1994; 5(1):39-44. PubMed ID: 8031534
[TBL] [Abstract][Full Text] [Related]
12. [Ring chromosome 13 (type I) 45,XY,-13/46, XY,r(13)(p11:q34)].
Díaz-Cardama Sousa I; Mora Gandarillas I; Vázquez Rodríguez M; Viso Lorenzo A; Alonso Villa MJ; Fernández Toral J
An Esp Pediatr; 1990 Jun; 32(6):556-8. PubMed ID: 2221637
[No Abstract] [Full Text] [Related]
13. Mosaic 45,xy,-21/46,xy in a child with G deletion syndrome I.
Olinici CD; Butnariu J; Popescu A; Giurguiman M
Ann Genet; 1977 Jun; 20(2):115-7. PubMed ID: 302684
[TBL] [Abstract][Full Text] [Related]
14. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
Leichtman LG; Zackowski JL; Storto PD; Newlin A
Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648
[TBL] [Abstract][Full Text] [Related]
15. Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2).
Legius E; Fryns JP; Eyskens B; Eggermont E; Desmet V; de Bethune G; Van den Berghe H
Am J Med Genet; 1990 Apr; 35(4):532-5. PubMed ID: 2333885
[TBL] [Abstract][Full Text] [Related]
16. Molecular and cytogenetic characterization of 9p- abnormalities.
Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
[TBL] [Abstract][Full Text] [Related]
17. Male with mosaicism for supernumerary ring X chromosome: analysis of phenotype and characterization of genotype using array comparative genome hybridization.
Baker PR; Tsai AC; Springer M; Swisshelm K; March J; Brown K; Bellus G
J Craniofac Surg; 2010 Sep; 21(5):1369-75. PubMed ID: 20856023
[TBL] [Abstract][Full Text] [Related]
18. Choanal atresia in a patient with the deletion (9p) syndrome.
Shashi V; Golden WL; Fryburg JS
Am J Med Genet; 1994 Jan; 49(1):88-90. PubMed ID: 8172257
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 46,XY del(18)(q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome.
Maaswinkel-Mooij PD; de Jong P; Beverstock GC
Clin Genet; 1993 Feb; 43(2):76-8. PubMed ID: 8448905
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
