Thomas GH - Search Results

1

Thomas GH, Thomas B, Trachtenberg SW. Thomas GH, et al. Among authors: thomas b. Pediatr Clin North Am. 1993 Jun;40(3):675-83. doi: 10.1016/s0031-3955(16)38558-3. Pediatr Clin North Am. 1993. PMID: 8493068

2

Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousins.

Doheny KF, Rasmussen SA, Rutberg J, Semenza GL, Stamberg J, Schwartz M, Batista DA, Stetten G, Thomas GH. Doheny KF, et al. Among authors: thomas gh. Am J Med Genet. 1997 Mar 17;69(2):188-93. Am J Med Genet. 1997. PMID: 9056559

3

"Pseudodeficiencies" of lysosomal hydrolases.

Thomas GH. Thomas GH. Am J Hum Genet. 1994 Jun;54(6):934-40. Am J Hum Genet. 1994. PMID: 7911004 Free PMC article. Review. No abstract available.

4

Chromosomal disorders: background and neuroradiology.

Kumar AJ, Naidich TP, Stetten G, Reiss AL, Wang H, Thomas GH, Hurko O. Kumar AJ, et al. Among authors: thomas gh. AJNR Am J Neuroradiol. 1992 Mar-Apr;13(2):577-93. AJNR Am J Neuroradiol. 1992. PMID: 1533086 Free PMC article. Review. No abstract available.

5

Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.

Migeon BR, Dunn MA, Thomas G, Schmeckpeper BJ, Naidu S. Migeon BR, et al. Am J Hum Genet. 1995 Mar;56(3):647-53. Am J Hum Genet. 1995. PMID: 7887418 Free PMC article.

6

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

Antonarakis SE, Blouin JL, Maher J, Avramopoulos D, Thomas G, Talbot CC Jr. Antonarakis SE, et al. Am J Hum Genet. 1993 Jun;52(6):1145-52. Am J Hum Genet. 1993. PMID: 8503447 Free PMC article.

7

Molecular cytogenetic evaluation in a patient with a translocation (3;21) associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES).

Praphanphoj V, Goodman BK, Thomas GH, Niel KM, Toomes C, Dixon MJ, Geraghty MT. Praphanphoj V, et al. Among authors: thomas gh. Genomics. 2000 Apr 1;65(1):67-9. doi: 10.1006/geno.2000.6157. Genomics. 2000. PMID: 10777667 Free article.

8

Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome.

Goodman BK, Rutberg J, Lin WW, Pulver AE, Thomas GH. Goodman BK, et al. Among authors: thomas gh. J Inherit Metab Dis. 2000 Dec;23(8):847-8. doi: 10.1023/a:1026773005303. J Inherit Metab Dis. 2000. PMID: 11196113 No abstract available.

9

Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndrome.

Sigurdardottir S, Goodman BK, Rutberg J, Thomas GH, Jabs EW, Geraghty MT. Sigurdardottir S, et al. Among authors: thomas gh. Am J Med Genet. 1999 Dec 22;87(5):384-90. doi: 10.1002/(sici)1096-8628(19991222)87:5<384::aid-ajmg3>3.0.co;2-r. Am J Med Genet. 1999. PMID: 10594875

10

A novel variant three-way translocation of inversion 16 in a case of AML-M4eo following low dose methotrexate therapy.

Li S, Couzi RJ, Thomas GH, Friedman AD, Borowitz MJ. Li S, et al. Among authors: thomas gh. Cancer Genet Cytogenet. 2001 Feb;125(1):74-7. doi: 10.1016/s0165-4608(00)00360-5. Cancer Genet Cytogenet. 2001. PMID: 11297772

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