204 related articles for article (PubMed ID: 2074558)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Alagille syndrome with interstitial 20p deletion derived from maternal ins(7;20).
Li PH; Shu SG; Yang CH; Lo FC; Wen MC; Chi CS
Am J Med Genet; 1996 Jun; 63(4):537-41. PubMed ID: 8826431
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Deletions of 20p12 in Alagille syndrome: frequency and molecular characterization.
Krantz ID; Rand EB; Genin A; Hunt P; Jones M; Louis AA; Graham JM; Bhatt S; Piccoli DA; Spinner NB
Am J Med Genet; 1997 May; 70(1):80-6. PubMed ID: 9129746
[TBL] [Abstract][Full Text] [Related]
10. Apparent Greig cephalopolysyndactyly and sinus node disease.
Fryns JP; De Waele P; Van der Hauwaert L; Van den Berghe H
Am J Med Genet; 1993 Jan; 45(1):38-40. PubMed ID: 8418656
[TBL] [Abstract][Full Text] [Related]
11. Interstitial deletion of 11q.
Guć-Sćekić M; Pilić-Radivojević G; Mrdjenović G; Djurić M
J Med Genet; 1989 Mar; 26(3):205-6. PubMed ID: 2468775
[No Abstract] [Full Text] [Related]
12. Interstitial deletion del(2)(q24q31) with a phenotype similar to del(2)(q31q33).
Wamsler C; Müller B; Freyberger G; Schmid M
Am J Med Genet; 1991 May; 39(2):204-6. PubMed ID: 2063926
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
Stratton RF; Dobyns WB; Greenberg F; DeSana JB; Moore C; Fidone G; Runge GH; Feldman P; Sekhon GS; Pauli RM
Am J Med Genet; 1986 Jul; 24(3):421-32. PubMed ID: 3728561
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. A case of deletion 14(q22.1-->q22.3) associated with anophthalmia and pituitary abnormalities.
Elliott J; Maltby EL; Reynolds B
J Med Genet; 1993 Mar; 30(3):251-2. PubMed ID: 7682620
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Interstitial deletion del(17) (q21.3q23 or 24.2) syndrome.
Dallapiccola B; Mingarelli R; Digilio C; Obregon MG; Giannotti A
Clin Genet; 1993 Jan; 43(1):54-5. PubMed ID: 8462199
[No Abstract] [Full Text] [Related]
20. A case of a female infant with simultaneous occurrence of de novo terminal deletions on chromosome 14q and 20p.
Uehara S; Akai Y; Takeyama Y; Okamura K; Takabayashi T; Yajima A; Natsui M; Nakai H
Clin Genet; 1993 Jan; 43(1):28-33. PubMed ID: 8179640
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]