173 related articles for article (PubMed ID: 2705486)
1. Deletion of terminal portion of 6q: report of a case with unusual malformations.
Shen-Schwarz S; Hill LM; Surti U; Marchese S
Am J Med Genet; 1989 Jan; 32(1):81-6. PubMed ID: 2705486
[TBL] [Abstract][Full Text] [Related]
2. New insights into the phenotypes of 6q deletions.
Hopkin RJ; Schorry E; Bofinger M; Milatovich A; Stern HJ; Jayne C; Saal HM
Am J Med Genet; 1997 Jun; 70(4):377-86. PubMed ID: 9182778
[TBL] [Abstract][Full Text] [Related]
3. Deletion of proximal 6q: a clinical report and review of the literature.
Yamamoto Y; Okamoto N; Shiraishi H; Yanagisawa M; Kamoshita S
Am J Med Genet; 1986 Nov; 25(3):467-71. PubMed ID: 3789009
[TBL] [Abstract][Full Text] [Related]
4. Chromosome 6q deletions: a report of two additional cases and a review of the literature.
McLeod DR; Fowlow SB; Robertson A; Samcoe D; Burgess I; Hoo JJ
Am J Med Genet; 1990 Jan; 35(1):79-84. PubMed ID: 2405671
[TBL] [Abstract][Full Text] [Related]
5. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.
Casaccia G; Mobili L; Braguglia A; Santoro F; Bagolan P
Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):210-3. PubMed ID: 16498629
[TBL] [Abstract][Full Text] [Related]
6. Report of two cases of distal deletion of the long arm of chromosome 6.
Stevens CA; Fineman RM; Breg WR; Silken AB
Am J Med Genet; 1988 Apr; 29(4):807-14. PubMed ID: 3400725
[TBL] [Abstract][Full Text] [Related]
7. Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37).
Wang TH; Johnston K; Hsieh CL; Dennery PA
Am J Med Genet; 1994 Feb; 49(4):399-401. PubMed ID: 8160733
[TBL] [Abstract][Full Text] [Related]
8. Terminal deletion 6p23: a case report.
Kormann-Bortolotto MH; Farah LM; Soares D; Corbani M; Müller R; Adell AC
Am J Med Genet; 1990 Dec; 37(4):475-7. PubMed ID: 2260591
[TBL] [Abstract][Full Text] [Related]
9. Interstitial deletion (6)q13q15.
Gershoni-Baruch R; Mandel H; Bar El H; Bar-Nizan N; Borochowitz Z; Dar H
Am J Med Genet; 1996 Apr; 62(4):345-7. PubMed ID: 8723062
[TBL] [Abstract][Full Text] [Related]
10. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
[TBL] [Abstract][Full Text] [Related]
11. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW
Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia.
Hatem E; Meriam BR; Walid D; Adenen M; Moez G; Ali S
Prenat Diagn; 2007 May; 27(5):471-4. PubMed ID: 17380471
[TBL] [Abstract][Full Text] [Related]
13. Del(14)(q22.1q23.2) in a patient with anophthalmia and pituitary hypoplasia.
Lemyre E; Lemieux N; Décarie JC; Lambert M
Am J Med Genet; 1998 May; 77(2):162-5. PubMed ID: 9605291
[TBL] [Abstract][Full Text] [Related]
14. Monosomy 11q: report of two familial cases and review of the literature.
Hustinx R; Verloes A; Grattagliano B; Herens C; Jamar M; Soyeur D; Schaaps JP; Koulischer L
Am J Med Genet; 1993 Sep; 47(3):312-7. PubMed ID: 8135272
[TBL] [Abstract][Full Text] [Related]
15. Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations.
Ramer JC; Mowrey PN; Robins DB; Ligato S; Towfighi J; Ladda RL
Am J Med Genet; 1990 Nov; 37(3):392-400. PubMed ID: 2260571
[TBL] [Abstract][Full Text] [Related]
16. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
Kara N; Okten G; Guneş SO; Saglam Y; Tasdemir HA; Pinarli FA
Epilepsy Res; 2008 Aug; 80(2-3):219-23. PubMed ID: 18485670
[TBL] [Abstract][Full Text] [Related]
17. Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].
Chitayat D; Babul R; Silver MM; Jay V; Teshima IE; Babyn P; Becker LE
Am J Med Genet; 1996 Jan; 61(1):45-8. PubMed ID: 8741917
[TBL] [Abstract][Full Text] [Related]
18. Interstitial deletion of the long arm of chromosome 6 associated with unusual limb anomalies: report of two new patients and review of the literature.
Pandya A; Braverman N; Pyeritz RE; Ying KL; Kline AD; Falk RE
Am J Med Genet; 1995 Oct; 59(1):38-43. PubMed ID: 8849008
[TBL] [Abstract][Full Text] [Related]
19. Nonrandom association of atrioventricular canal and del (8p) syndrome.
Marino B; Reale A; Giannotti A; Digilio MC; Dallapiccola B
Am J Med Genet; 1992 Feb; 42(4):424-7. PubMed ID: 1609823
[TBL] [Abstract][Full Text] [Related]
20. Ocular anomalies associated with interstitial deletion of chromosome 2q31: case report and review.
Gambrelle J; Till M; Lukusa B; Beby F; Mory N; Sann L; Kodjikian L; Grange JD; Putet G
Ophthalmic Genet; 2007 Jun; 28(2):105-9. PubMed ID: 17558854
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]