108 related articles for article (PubMed ID: 7521123)
21. A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21.
Motegi T; Ohuchi M; Ohtaki C; Fujiwara K; Enomoto S; Hasegawa T; Kishi K; Hayakawa H
Hum Genet; 1985; 71(2):160-2. PubMed ID: 4043965
[TBL] [Abstract][Full Text] [Related]
22. A report of a patient with duplication of 7p13-->pter and deletion of 2p23-->pter due to a maternal 2p;7p translocation.
Türköver BB; Sayar C; Toksoy G; Elçioğlu N
Turk J Pediatr; 2009; 51(2):174-9. PubMed ID: 19480332
[TBL] [Abstract][Full Text] [Related]
23. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
Cai T; Yu P; Tagle DA; Xia J
Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
[TBL] [Abstract][Full Text] [Related]
24. De novo terminal deletion 7p22.1--pter in a child without craniosynostosis.
Speleman F; Craen M; Leroy J
J Med Genet; 1989 Aug; 26(8):528-32. PubMed ID: 2671374
[TBL] [Abstract][Full Text] [Related]
25. Is loss of band 7p21 really critical for manifestation of craniosynostosis in 7p-?
Kikkawa K; Narahara K; Tsuji K; Kubo T; Yokoyama Y; Seino Y
Am J Med Genet; 1993 Jan; 45(1):108-10. PubMed ID: 8418642
[No Abstract] [Full Text] [Related]
26. Recurrent deletions involving chromosomes 1, 5, 17, and 18 in colorectal carcinoma: possible role in biological and clinical behavior of tumors.
Gerdes H; Chen Q; Elahi AH; Sircar A; Goldberg E; Winawer D; Urmacher C; Winawer SJ; Jhanwar SC
Anticancer Res; 1995; 15(1):13-24. PubMed ID: 7733622
[TBL] [Abstract][Full Text] [Related]
27. Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours.
Perotti D; Testi MA; Mondini P; Pilotti S; Green ED; Pession A; Sozzi G; Pierotti MA; Fossati-Bellani F; Radice P
Genes Chromosomes Cancer; 2001 May; 31(1):42-7. PubMed ID: 11284034
[TBL] [Abstract][Full Text] [Related]
28. Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7p.
Lewanda AF; Cohen MM; Jackson CE; Taylor EW; Li X; Beloff M; Day D; Clarren SK; Ortiz R; Garcia C
Genomics; 1994 Jan; 19(1):115-9. PubMed ID: 8188211
[TBL] [Abstract][Full Text] [Related]
29. Evidence for two tumor suppressor loci associated with proximal chromosome 9p to q and distal chromosome 9q in bladder cancer and the initial screening for GAS1 and PTC mutations.
Simoneau AR; Spruck CH; Gonzalez-Zulueta M; Gonzalgo ML; Chan MF; Tsai YC; Dean M; Steven K; Horn T; Jones PA
Cancer Res; 1996 Nov; 56(21):5039-43. PubMed ID: 8895761
[TBL] [Abstract][Full Text] [Related]
30. A fetus with an abnormal chromosome 7 and possible hydrolethalus syndrome.
Seller MJ; Pal K; Docherty Z; Nash TG
Clin Dysmorphol; 1994 Jan; 3(1):35-9. PubMed ID: 8205324
[TBL] [Abstract][Full Text] [Related]
31. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
[TBL] [Abstract][Full Text] [Related]
32. Molecular and cytogenetic characterization of 9p- abnormalities.
Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
[TBL] [Abstract][Full Text] [Related]
33. A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigation.
Bilguvar K; Bydon M; Bayrakli F; Ercan-Sencicek AG; Bayri Y; Mason C; DiLuna ML; Seashore M; Bronen R; Lifton RP; State M; Gunel M
J Neurosurg; 2007 Dec; 107(6 Suppl):495-9. PubMed ID: 18154020
[TBL] [Abstract][Full Text] [Related]
34. Chromosome 7 short arm deletion, 7p21----pter.
Schömig-Spingler M; Schmid M; Brosi W; Grimm T
Hum Genet; 1986 Nov; 74(3):323-5. PubMed ID: 3781561
[TBL] [Abstract][Full Text] [Related]
35. Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene region.
Vortkamp A; Gessler M; Le Paslier D; Elaswarapu R; Smith S; Grzeschik KH
Genomics; 1994 Aug; 22(3):563-8. PubMed ID: 8001967
[TBL] [Abstract][Full Text] [Related]
36. [7p14.1 microdeletion and Greig cephalopolysyndactyly syndrome].
Montoro Cremades D; Manchón Trives I; Botella López V; Alcaraz Más L; García Martínez MR; Galán Sánchez F
An Pediatr (Barc); 2011 Apr; 74(4):266-9. PubMed ID: 21296629
[TBL] [Abstract][Full Text] [Related]
37. Saethre-Chotzen syndrome with severe developmental delay associated with deletion of chromosomic region 7p15 --> pter.
Touliatou V; Mavrou A; Kolialexi A; Kanavakis E; Kitsiou-Tzeli S
Genet Couns; 2007; 18(3):295-301. PubMed ID: 18019370
[TBL] [Abstract][Full Text] [Related]
38. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
Harvard C; Malenfant P; Koochek M; Creighton S; Mickelson EC; Holden JJ; Lewis ME; Rajcan-Separovic E
Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
[TBL] [Abstract][Full Text] [Related]
39. Interstitial deletion of 2q associated with craniosynostosis, ocular coloboma, and limb abnormalities: cytogenetic and molecular investigation.
Nixon J; Oldridge M; Wilkie AO; Smith K
Am J Med Genet; 1997 Jun; 70(3):324-7. PubMed ID: 9188674
[TBL] [Abstract][Full Text] [Related]
40. Craniosynostosis in an infant with an interstitial deletion of 15q [46,XY,del(15)(q15q22.1)].
Fukushima Y; Wakui K; Nishida T; Nishimoto H
Am J Med Genet; 1990 Jun; 36(2):209-13. PubMed ID: 2368808
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
