Fischel-Ghodsian N - Search Results

1

Prenatal diagnosis and dysmorphic findings in mosaic trisomy 16.

Garber A, Carlson D, Schreck R, Fischel-Ghodsian N, Hsu WT, Oeztas S, Pepkowitz S, Graham JM Jr. Garber A, et al. Prenat Diagn. 1994 Apr;14(4):257-66. doi: 10.1002/pd.1970140405. Prenat Diagn. 1994. PMID: 8066035

2

Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literature.

Bacino CA, Schreck R, Fischel-Ghodsian N, Pepkowitz S, Prezant TR, Graham JM Jr. Bacino CA, et al. Am J Med Genet. 1995 May 8;56(4):359-65. doi: 10.1002/ajmg.1320560404. Am J Med Genet. 1995. PMID: 7604844 Review.

3

Transient leukemia with trisomy 21: description of a case and review of the literature.

Bhatt S, Schreck R, Graham JM, Korenberg JR, Hurvitz CG, Fischel-Ghodsian N. Bhatt S, et al. Am J Med Genet. 1995 Sep 25;58(4):310-4. doi: 10.1002/ajmg.1320580404. Am J Med Genet. 1995. PMID: 8533839 Review.

4

Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases.

Hsu WT, Shchepin DA, Mao R, Berry-Kravis E, Garber AP, Fischel-Ghodsian N, Falk RE, Carlson DE, Roeder ER, Leeth EA, Hajianpour MJ, Wang JC, Rosenblum-Vos LS, Bhatt SD, Karson EM, Hux CH, Trunca C, Bialer MG, Linn SK, Schreck RR. Hsu WT, et al. Am J Med Genet. 1998 Dec 28;80(5):473-80. doi: 10.1002/(sici)1096-8628(19981228)80:5<473::aid-ajmg7>3.0.co;2-a. Am J Med Genet. 1998. PMID: 9880211

5

Regional mapping of the gene for familial Mediterranean fever on human chromosome 16p13.

Fischel-Ghodsian N, Bu X, Prezant TR, Oeztas S, Huang ZS, Bohlman MC, Rotter JI, Shohat M. Fischel-Ghodsian N, et al. Am J Med Genet. 1993 Jul 1;46(6):689-93. doi: 10.1002/ajmg.1320460619. Am J Med Genet. 1993. PMID: 8362911

6

Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome.

Fischel-Ghodsian N, Bohlman MC, Prezant TR, Graham JM Jr, Cederbaum SD, Edwards MJ. Fischel-Ghodsian N, et al. Pediatr Res. 1992 Jun;31(6):557-60. doi: 10.1203/00006450-199206000-00004. Pediatr Res. 1992. PMID: 1635816

7

Prenatal diagnosis of hemoglobinopathies.

Fischel-Ghodsian N. Fischel-Ghodsian N. Clin Perinatol. 1990 Dec;17(4):811-28. Clin Perinatol. 1990. PMID: 2286030 Review.

8

Linkage of Crohn's disease to the major histocompatibility complex region is detected by multiple non-parametric analyses.

Yang H, Plevy SE, Taylor K, Tyan D, Fischel-Ghodsian N, McElree C, Targan SR, Rotter JI. Yang H, et al. Gut. 1999 Apr;44(4):519-26. doi: 10.1136/gut.44.4.519. Gut. 1999. PMID: 10075959 Free PMC article.

9

Characterization of the human mitochondrial ribosomal S12 gene.

Johnson DF, Hamon M, Fischel-Ghodsian N. Johnson DF, et al. Genomics. 1998 Sep 15;52(3):363-8. doi: 10.1006/geno.1998.5448. Genomics. 1998. PMID: 9790755

10

Additional evidence of linkage between Crohn's disease and a putative locus on chromosome 12.

Yang H, Ohmen JD, Ma Y, Bentley LG, Targan SR, Fischel-Ghodsian N, Rotter JI. Yang H, et al. Genet Med. 1999 Jul-Aug;1(5):194-8. doi: 10.1097/00125817-199907000-00005. Genet Med. 1999. PMID: 11256672 Free article.

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