352 related articles for article (PubMed ID: 3728561)
1. 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]
2. Interstitial deletion of (17)(p11.2p11.2) in nine patients.
Smith AC; McGavran L; Robinson J; Waldstein G; Macfarlane J; Zonona J; Reiss J; Lahr M; Allen L; Magenis E
Am J Med Genet; 1986 Jul; 24(3):393-414. PubMed ID: 2425619
[TBL] [Abstract][Full Text] [Related]
3. Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del (17)(p11.2p11.2).
Kondo I; Matsuura S; Kuwajima K; Tokashiki M; Izumikawa Y; Naritomi K; Niikawa N; Kajii T
Am J Med Genet; 1991 Nov; 41(2):225-9. PubMed ID: 1785639
[TBL] [Abstract][Full Text] [Related]
4. Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature.
Fischer H; Oswald HP; Duba HC; Doczy L; Simma B; Utermann G; Haas OA
Klin Padiatr; 1993; 205(3):162-6. PubMed ID: 8350589
[TBL] [Abstract][Full Text] [Related]
5. 7p deletion syndrome: an adult with mild manifestations.
Grebe TA; Stevens MA; Byrne-Essif K; Cassidy SB
Am J Med Genet; 1992 Sep; 44(1):18-23. PubMed ID: 1519644
[TBL] [Abstract][Full Text] [Related]
6. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4.
Beall MH; Falk RE; Ying KL
Am J Med Genet; 1988 Nov; 31(3):553-7. PubMed ID: 3067576
[TBL] [Abstract][Full Text] [Related]
7. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
Lin AE; Garver KL; Diggans G; Clemens M; Wenger SL; Steele MW; Jones MC; Israel J
Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
[TBL] [Abstract][Full Text] [Related]
8. Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases.
Poissonnier M; Turleau C; Olivier-Martin M; Milleret-Proyart MJ; Prieur M; Dubos M; Cabanis MO; Mugneret F; Blanc P; Noel L
Ann Genet; 1992; 35(3):146-51. PubMed ID: 1466563
[TBL] [Abstract][Full Text] [Related]
9. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
Wilson MG; Towner JW; Forsman I; Siris E
Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629
[TBL] [Abstract][Full Text] [Related]
10. Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q.
Thomas JA; Manchester DK; Prescott KE; Milner R; McGavran L; Cohen MM
Am J Med Genet; 1996 Apr; 62(4):372-5. PubMed ID: 8723067
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
Chitayat D; Ruvalcaba RH; Babul R; Teshima IE; Posnick JC; Vekemans MJ; Scarpelli H; Thuline H
Am J Med Genet; 1995 Jan; 55(2):147-54. PubMed ID: 7717413
[TBL] [Abstract][Full Text] [Related]
13. Interstitial deletion of long arm of chromosome 13.
Carnevale A; Frias S; Alcantar R
Ann Genet; 1984; 27(1):49-52. PubMed ID: 6609673
[TBL] [Abstract][Full Text] [Related]
14. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
15. Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.
Fryburg JS; Golden WL
Am J Med Genet; 1993 Mar; 45(5):638-41. PubMed ID: 7681252
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Interstitial deletion of (17)(p11.2). A microdeletion syndrome. Another example.
de Almeida JC; Reis DF; Martins RR
Ann Genet; 1989; 32(3):184-6. PubMed ID: 2817780
[TBL] [Abstract][Full Text] [Related]
18. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
Copelli S; del Rey G; Heinrich J; Coco R
Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102
[TBL] [Abstract][Full Text] [Related]
19. Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
White DM; Pillers DA; Reiss JA; Brown MG; Magenis RE
Am J Med Genet; 1995 Jul; 57(4):588-97. PubMed ID: 7573135
[TBL] [Abstract][Full Text] [Related]
20. Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome.
Ioan DM; Maximilian C; Kleczkowska A; Fryns JP
Ann Genet; 1992; 35(3):167-9. PubMed ID: 1466567
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]