Morrow BE - Search Results

1

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome.

Matsuoka R, Kimura M, Scambler PJ, Morrow BE, Imamura S, Minoshima S, Shimizu N, Yamagishi H, Joh-o K, Watanabe S, Oyama K, Saji T, Ando M, Takao A, Momma K. Matsuoka R, et al. Among authors: morrow be. Hum Genet. 1998 Jul;103(1):70-80. doi: 10.1007/s004390050786. Hum Genet. 1998. PMID: 9737780

2

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.

Carlson C, Sirotkin H, Pandita R, Goldberg R, McKie J, Wadey R, Patanjali SR, Weissman SM, Anyane-Yeboa K, Warburton D, Scambler P, Shprintzen R, Kucherlapati R, Morrow BE. Carlson C, et al. Among authors: morrow be. Am J Hum Genet. 1997 Sep;61(3):620-9. doi: 10.1086/515508. Am J Hum Genet. 1997. PMID: 9326327 Free PMC article.

3

Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.

Morrow B, Goldberg R, Carlson C, Das Gupta R, Sirotkin H, Collins J, Dunham I, O'Donnell H, Scambler P, Shprintzen R, et al. Morrow B, et al. Am J Hum Genet. 1995 Jun;56(6):1391-403. Am J Hum Genet. 1995. PMID: 7762562 Free PMC article.

4

Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region.

O'Donnell H, McKeown C, Gould C, Morrow B, Scambler P. O'Donnell H, et al. Am J Hum Genet. 1997 Jun;60(6):1544-8. doi: 10.1016/S0002-9297(07)64250-5. Am J Hum Genet. 1997. PMID: 9199579 Free PMC article. No abstract available.

5

Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.

Carlson C, Papolos D, Pandita RK, Faedda GL, Veit S, Goldberg R, Shprintzen R, Kucherlapati R, Morrow B. Carlson C, et al. Am J Hum Genet. 1997 Apr;60(4):851-9. Am J Hum Genet. 1997. PMID: 9106531 Free PMC article.

6

Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndrome.

Sirotkin H, Morrow B, DasGupta R, Goldberg R, Patanjali SR, Shi G, Cannizzaro L, Shprintzen R, Weissman SM, Kucherlapati R. Sirotkin H, et al. Hum Mol Genet. 1996 May;5(5):617-24. doi: 10.1093/hmg/5.5.617. Hum Mol Genet. 1996. PMID: 8733128

7

Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome.

Sirotkin H, O'Donnell H, DasGupta R, Halford S, St Jore B, Puech A, Parimoo S, Morrow B, Skoultchi A, Weissman SM, Scambler P, Kucherlapati R. Sirotkin H, et al. Genomics. 1997 Apr 1;41(1):75-83. doi: 10.1006/geno.1997.4627. Genomics. 1997. PMID: 9126485 Free article.

8

A common molecular basis for rearrangement disorders on chromosome 22q11.

Edelmann L, Pandita RK, Spiteri E, Funke B, Goldberg R, Palanisamy N, Chaganti RS, Magenis E, Shprintzen RJ, Morrow BE. Edelmann L, et al. Among authors: morrow be. Hum Mol Genet. 1999 Jul;8(7):1157-67. doi: 10.1093/hmg/8.7.1157. Hum Mol Genet. 1999. PMID: 10369860

9

Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.

Funke B, Edelmann L, McCain N, Pandita RK, Ferreira J, Merscher S, Zohouri M, Cannizzaro L, Shanske A, Morrow BE. Funke B, et al. Among authors: morrow be. Am J Hum Genet. 1999 Mar;64(3):747-58. doi: 10.1086/302284. Am J Hum Genet. 1999. PMID: 10053009 Free PMC article.

10

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

Edelmann L, Pandita RK, Morrow BE. Edelmann L, et al. Among authors: morrow be. Am J Hum Genet. 1999 Apr;64(4):1076-86. doi: 10.1086/302343. Am J Hum Genet. 1999. PMID: 10090893 Free PMC article.

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