Haddad B - Search Results

1

Cytogenetic and molecular cytogenetic studies of a case of interstitial deletion of proximal 15q.

Tonk V, Wyandt HE, Osella P, Skare J, Wu BL, Haddad B, Milunsky A. Tonk V, et al. Among authors: haddad b. Clin Genet. 1995 Sep;48(3):151-5. doi: 10.1111/j.1399-0004.1995.tb04076.x. Clin Genet. 1995. PMID: 8556823 Review.

2

Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).

Haddad BR, Lin AE, Wyandt H, Milunsky A. Haddad BR, et al. J Med Genet. 1996 Dec;33(12):1045-7. doi: 10.1136/jmg.33.12.1045. J Med Genet. 1996. PMID: 9004142 Free PMC article.

3

Evaluation of satellited Y chromosome (Yqs) detected during prenatal diagnosis.

Haddad BR, Huang Y, Wyandt H, Milunsky A. Haddad BR, et al. Acta Obstet Gynecol Scand. 1997 Mar;76(3):281-3. Acta Obstet Gynecol Scand. 1997. PMID: 9093147 No abstract available.

4

Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region.

Rizzu P, Haddad BR, Vallcorba I, Alonso A, Ferro MT, Garcia-Sagredo JM, Baldini A. Rizzu P, et al. Among authors: haddad br. Am J Med Genet. 1997 Feb 11;68(4):428-32. Am J Med Genet. 1997. PMID: 9021016

5

Identification of de novo chromosomal markers and derivatives by spectral karyotyping.

Haddad BR, Schröck E, Meck J, Cowan J, Young H, Ferguson-Smith MA, du Manoir S, Ried T. Haddad BR, et al. Hum Genet. 1998 Nov;103(5):619-25. doi: 10.1007/s004390050878. Hum Genet. 1998. PMID: 9860306

6

Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype.

Bendavid C, Haddad BR, Griffin A, Huizing M, Dubourg C, Gicquel I, Cavalli LR, Pasquier L, Shanske AL, Long R, Ouspenskaia M, Odent S, Lacbawan F, David V, Muenke M. Bendavid C, et al. Among authors: haddad br. J Med Genet. 2006 Jun;43(6):496-500. doi: 10.1136/jmg.2005.037176. Epub 2005 Sep 30. J Med Genet. 2006. PMID: 16199538 Free PMC article.

7

FISH diagnosis of the common 57-kb deletion in CTNS causing cystinosis.

Bendavid C, Kleta R, Long R, Ouspenskaia M, Muenke M, Haddad BR, Gahl WA. Bendavid C, et al. Hum Genet. 2004 Nov;115(6):510-4. doi: 10.1007/s00439-004-1170-2. Epub 2004 Sep 9. Hum Genet. 2004. PMID: 15365816

8

Mapping segmental imbalances using comparative genomic hybridization and eigenanalysis.

Haddad B, Antonacci R, Rizzu P, Lindsay EA, Hughes MR, Smith LC, Knapp RD, Baldini A. Haddad B, et al. Cytogenet Cell Genet. 1995;71(3):276-9. doi: 10.1159/000134126. Cytogenet Cell Genet. 1995. PMID: 7587393

9

Holoprosencephaly-Polydactyly syndrome: in search of an etiology.

Cordero DR, Bendavid C, Shanske AL, Haddad BR, Muenke M. Cordero DR, et al. Eur J Med Genet. 2008 Mar-Apr;51(2):106-12. doi: 10.1016/j.ejmg.2007.08.004. Epub 2007 Sep 15. Eur J Med Genet. 2008. PMID: 18178536 Free PMC article.

10

Comprehensive cytogenetic evaluation of a mature ovarian teratoma case.

Schmid-Braz AT, Cavalli LR, Cornélio DA, Wuicik L, Ribeiro EM, Bleggi-Torres LF, Lima RS, de Andrade Urban C, Haddad BR, Cavalli IJ. Schmid-Braz AT, et al. Cancer Genet Cytogenet. 2002 Jan 15;132(2):165-8. doi: 10.1016/s0165-4608(01)00562-3. Cancer Genet Cytogenet. 2002. PMID: 11850083

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