371 related articles for article (PubMed ID: 9298747)
1. Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient.
Caliebe A; Waltz S; Jenderny J
Clin Genet; 1997 Aug; 52(2):116-9. PubMed ID: 9298747
[TBL] [Abstract][Full Text] [Related]
2. Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
Descartes M; Keppler-Noreuil K; Knops J; Longshore JW; Finley WH; Carroll AJ
Clin Genet; 1996 Dec; 50(6):538-40. PubMed ID: 9147894
[TBL] [Abstract][Full Text] [Related]
3. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
Davies J; Voullaire L; Bankier A
Ann Genet; 1990; 33(2):92-5. PubMed ID: 2241091
[TBL] [Abstract][Full Text] [Related]
4. Interstitial deletion of the short arm of chromosome 4.
Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
Stoll C; Levy J; Roth MP
J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Partial trisomy 15q: report of a patient and literature review.
Chandler K; Schrander-Stumpel CT; Engelen J; Theunissen P; Fryns JP
Genet Couns; 1997; 8(2):91-7. PubMed ID: 9219006
[TBL] [Abstract][Full Text] [Related]
8. New case of interstitial deletion 12(q15-q21.2) in a girl with facial dysmorphism and mental retardation.
Schluth C; Gesny R; Borck G; Redon R; Abadie V; Kleinfinger P; Munnich A; Lyonnet S; Colleaux L
Am J Med Genet A; 2008 Jan; 146A(1):93-6. PubMed ID: 18076123
[TBL] [Abstract][Full Text] [Related]
9. Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion.
Titomanlio L; Romano A; Conti A; Genesio R; Salerno M; De Brasi D; Nitsch L; Del Giudice E
Am J Med Genet A; 2004 Jun; 127A(2):197-200. PubMed ID: 15108211
[TBL] [Abstract][Full Text] [Related]
10. Rieger syndrome and interstitial 4q26 deletion.
Fryns JP; Van Den Berghe H
Genet Couns; 1992; 3(3):153-4. PubMed ID: 1388934
[No Abstract] [Full Text] [Related]
11. A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.
Wagstaff J; Hemann M
Am J Hum Genet; 1995 Jan; 56(1):302-9. PubMed ID: 7825591
[TBL] [Abstract][Full Text] [Related]
12. 16q21 is critical for 16q deletion syndrome.
Naritomi K; Shiroma N; Izumikawa Y; Sameshima K; Ohdo S; Hirayama K
Clin Genet; 1988 May; 33(5):372-5. PubMed ID: 3378367
[TBL] [Abstract][Full Text] [Related]
13. Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.
Shapira SK; McCaskill C; Northrup H; Spikes AS; Elder FF; Sutton VR; Korenberg JR; Greenberg F; Shaffer LG
Am J Hum Genet; 1997 Sep; 61(3):642-50. PubMed ID: 9326330
[TBL] [Abstract][Full Text] [Related]
14. A Novel 23.1 Mb Interstitial Deletion Involving 7q22.3q32.1 in a Girl with Short Stature, Motor Delay, and Craniofacial Dysmorphism.
Del Refugio Rivera-Vega M; Gómez-Del Angel LA; Valdes-Miranda JM; Pérez-Cabrera A; Gonzalez-Huerta LM; Toral-López J; Cuevas-Covarrubias S
Cytogenet Genome Res; 2015; 145(1):1-5. PubMed ID: 25870946
[TBL] [Abstract][Full Text] [Related]
15. Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients.
Martinet D; Filges I; Besuchet Schmutz N; Morris MA; Gaide AC; Dahoun S; Bottani A; Addor MC; Antonarakis SE; Beckmann JS; Béna F
Am J Med Genet A; 2008 Aug; 146A(16):2094-102. PubMed ID: 18629875
[TBL] [Abstract][Full Text] [Related]
16. A dysmorphic boy with 4qter deletion and 4q32.3-34.3 duplication: clinical, cytogenetic, and molecular findings.
Van Buggenhout G; Maas NM; Fryns JP; Vermeesch JR
Am J Med Genet A; 2004 Dec; 131(2):186-9. PubMed ID: 15523640
[TBL] [Abstract][Full Text] [Related]
17. Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome.
Herens C; Jamar M; Alvarez-Gonzalez ML; Lesenfants S; Lombet J; Bonnivert J; Koulischer L; Verloes A
Am J Med Genet; 1997 Dec; 73(2):127-31. PubMed ID: 9409861
[TBL] [Abstract][Full Text] [Related]
18. 46, XY, del (3) (pter-->p25) syndrome: further delineation of the clinical phenotype.
Benini D; Vino L; Vecchini S; Fanos V
Eur J Pediatr; 1999 Dec; 158(12):955-7. PubMed ID: 10592068
[TBL] [Abstract][Full Text] [Related]
19. [A new clinico-cytogenetic syndrome--a proximal deletion of the short arm of chromosome 17].
Zaletaev DV; Marincheva GS
Pediatriia; 1988; (11):82-4. PubMed ID: 3226810
[No Abstract] [Full Text] [Related]
20. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
