Crolla JA - Search Results

1

FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases.

Crolla JA, Long F, Rivera H, Dennis NR. Crolla JA, et al. Am J Med Genet. 1998 Feb 3;75(4):355-66. doi: 10.1002/(sici)1096-8628(19980203)75:4<355::aid-ajmg4>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9482641

2

A method for generating hybrids containing nonselected fragments of human chromosomes.

Benham F, Hart K, Crolla J, Bobrow M, Francavilla M, Goodfellow PN. Benham F, et al. Genomics. 1989 May;4(4):509-17. doi: 10.1016/0888-7543(89)90274-7. Genomics. 1989. PMID: 2744762

3

A complex rearrangement associated with sex reversal and the Wolf-Hirschhorn syndrome: a cytogenetic and molecular study.

Coles K, Mackenzie M, Crolla J, Harvey J, Starr J, Howard F, Jacobs P. Coles K, et al. J Med Genet. 1992 Jun;29(6):400-6. doi: 10.1136/jmg.29.6.400. J Med Genet. 1992. PMID: 1619635 Free PMC article.

4

Nonisotopic in situ hybridization. Clinical cytogenetics and gene mapping applications.

Adinolfi M, Crolla J. Adinolfi M, et al. Adv Hum Genet. 1994;22:187-255. Adv Hum Genet. 1994. PMID: 7762453 Review. No abstract available.

5

Functional Xp disomy and hypomelanosis of Ito.

Rivera H, Correa-Cerro LS, Robinson DO, Crolla JA. Rivera H, et al. Among authors: crolla ja. Arch Med Res. 2000 Jan-Feb;31(1):88-92. doi: 10.1016/s0188-4409(99)00081-8. Arch Med Res. 2000. PMID: 10767487

6

Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays.

Fiegler H, Gribble SM, Burford DC, Carr P, Prigmore E, Porter KM, Clegg S, Crolla JA, Dennis NR, Jacobs P, Carter NP. Fiegler H, et al. Among authors: crolla ja. J Med Genet. 2003 Sep;40(9):664-70. doi: 10.1136/jmg.40.9.664. J Med Genet. 2003. PMID: 12960211 Free PMC article.

7

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.

Huang B, Crolla JA, Christian SL, Wolf-Ledbetter ME, Macha ME, Papenhausen PN, Ledbetter DH. Huang B, et al. Among authors: crolla ja. Hum Genet. 1997 Jan;99(1):11-7. doi: 10.1007/s004390050301. Hum Genet. 1997. PMID: 9003485

8

Clinical outcomes of adjacent 1 segregation in a familial translocation t(8;18)(p21.3;p11.23).

Cockwell AE, James RS, Moore IE, Hatchwell E, Crolla JA. Cockwell AE, et al. Among authors: crolla ja. J Med Genet. 1996 Jun;33(6):515-7. doi: 10.1136/jmg.33.6.515. J Med Genet. 1996. PMID: 8782055 Free PMC article.

9

Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins.

Brémond-Gignac D, Gérard-Blanluet M, Copin H, Bitoun P, Baumann C, Crolla JA, Benzacken B, Verloes A. Brémond-Gignac D, et al. Among authors: crolla ja. Am J Med Genet A. 2005 May 1;134(4):422-5. doi: 10.1002/ajmg.a.30646. Am J Med Genet A. 2005. PMID: 15779023

10

A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype.

Maggouta F, Roberts SE, Dennis NR, Veltman MW, Crolla JA. Maggouta F, et al. Among authors: crolla ja. J Med Genet. 2003 Jul;40(7):e84. doi: 10.1136/jmg.40.7.e84. J Med Genet. 2003. PMID: 12843333 Free PMC article. No abstract available.

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