137 related articles for article (PubMed ID: 3712390)
1. Monosomy 8p: an easily overlooked syndrome.
Bröcker-Vriends AH; Mooij PD; van Bel F; Beverstock GC; van de Kamp JJ
J Med Genet; 1986 Apr; 23(2):153-4. PubMed ID: 3712390
[TBL] [Abstract][Full Text] [Related]
2. Deletion of the short arm of chromosome 9. A clinically recognisable entity.
Fryns JP; Pedersen JC; Duyck H; Fabry G; Van den Berghe H
Eur J Pediatr; 1980 Sep; 134(3):201-4. PubMed ID: 7428770
[TBL] [Abstract][Full Text] [Related]
3. Monosomy 13q32.3----qter: report of two cases.
Rivera H; González-Flores SA; Rivas F; Sánchez-Corona J; Moller M; Cantú JM
J Med Genet; 1985 Apr; 22(2):142-5. PubMed ID: 3989831
[TBL] [Abstract][Full Text] [Related]
4. Infant with del(3) (p25-pter): karyotype-phenotype correlation and review of previously reported cases.
Nienhaus H; Mau U; Zang KD
Am J Med Genet; 1992 Nov; 44(5):573-5. PubMed ID: 1481811
[TBL] [Abstract][Full Text] [Related]
5. The 8p-syndrome.
Ostergaard GZ; Tommerup N
Ann Genet; 1989; 32(2):87-91. PubMed ID: 2667457
[TBL] [Abstract][Full Text] [Related]
6. Terminal deletion of chromosome 10q and its clinical features.
Kogasaka R; Morohoshi T; Sawada Y; Fujiwara M
Acta Paediatr Jpn; 1990 Feb; 32(1):83-7. PubMed ID: 2109493
[TBL] [Abstract][Full Text] [Related]
7. Chromosome 7 short-arm interstitial deletion (p14).
Moedjono SJ; Funderburk SJ; Sparkes RS
Hum Genet; 1978 Oct; 44(1):51-7. PubMed ID: 711238
[TBL] [Abstract][Full Text] [Related]
8. [A difficult cytogenetic diagnosis of 4p monosomy].
Vittu G; Croquette MF; Boidein F; Cousin J
J Genet Hum; 1988 Jan; 36(1-2):75-82. PubMed ID: 3379382
[TBL] [Abstract][Full Text] [Related]
9. Alagille syndrome and deletion of 20p.
Anad F; Burn J; Matthews D; Cross I; Davison BC; Mueller R; Sands M; Lillington DM; Eastham E
J Med Genet; 1990 Dec; 27(12):729-37. PubMed ID: 2074558
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. An apparent de novo terminal deletion of chromosome 2 (pter----p24:).
Francis GL; Flannery DB; Byrd JR; Fisher ST
J Med Genet; 1990 Feb; 27(2):137-8. PubMed ID: 2319584
[No Abstract] [Full Text] [Related]
12. The 8p- syndrome.
Reiss JA; Brenes PM; Chamberlin J; Magenis RE; Lovrien EW
Hum Genet; 1979 Mar; 47(2):135-40. PubMed ID: 437781
[TBL] [Abstract][Full Text] [Related]
13. The phenotypic and cytogenetic spectrum of partial trisomy 9.
Wilson GN; Raj A; Baker D
Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
[TBL] [Abstract][Full Text] [Related]
14. Deletion of chromosome 1p: a short review.
Howard PJ; Porteus M
Clin Genet; 1990 Feb; 37(2):127-31. PubMed ID: 1968791
[TBL] [Abstract][Full Text] [Related]
15. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
Schimmenti LA; Higgins RR; Mendelsohn NJ; Casey TM; Steinberger J; Mammel MC; Wiesner GL
Am J Med Genet; 1995 May; 57(1):52-6. PubMed ID: 7645598
[TBL] [Abstract][Full Text] [Related]
16. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC
Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815
[TBL] [Abstract][Full Text] [Related]
17. 46,XX,15p+ documented as dup (17p) by fluorescence in situ hybridization.
Spinner NB; Biegel JA; Sovinsky L; McDonald-McGinn D; Rehberg K; Parmiter AH; Zackai EH
Am J Med Genet; 1993 Apr; 46(1):95-7. PubMed ID: 8494037
[TBL] [Abstract][Full Text] [Related]
18. Interstitial deletion of the distal long arm of chromosome 4.
Sarda P; Lefort G; Fryns JP; Humeau C; Rieu D
J Med Genet; 1992 Apr; 29(4):259-61. PubMed ID: 1583648
[TBL] [Abstract][Full Text] [Related]
19. Probable de novo 17q duplication (q11.2-->q21.1): a newly recognised chromosomal syndrome in a child with Klinefelter's syndrome.
Butt AM; Mehta D; Goodeve JA; Flinter FA
J Med Genet; 1993 May; 30(5):436-7. PubMed ID: 8320713
[TBL] [Abstract][Full Text] [Related]
20. De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.
Fryns JP; Haspeslagh M; Agneessens A; van den Berghe H
Ann Genet; 1985; 28(1):45-8. PubMed ID: 3874588
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
