Thomas IT - Search Results

Year	Number of Results
1974	3
1975	1
1977	1
1986	3
1987	4
1988	2
1989	4
1991	2
1992	1
1993	7
1995	1
2000	1
2024	1
2025	1

1

Thomas IT, Frias JL, Felix V, Sanchez de Leon L, Hernandez RA, Jones MC. Thomas IT, et al. Am J Med Genet. 1986 Sep;25(1):85-98. doi: 10.1002/ajmg.1320250111. Am J Med Genet. 1986. PMID: 3099574 Review.

2

Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.

Jurgens JA, Barry BJ, Chan WM, MacKinnon S, Whitman MC, Matos Ruiz PM, Pratt BM, England EM, Pais L, Lemire G, Groopman E, Glaze C, Russell KA, Singer-Berk M, Di Gioia SA, Lee AS, Andrews C, Shaaban S, Wirth MM, Bekele S, Toffoloni M, Bradford VR, Foster EE, Berube L, Rivera-Quiles C, Mensching FM, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Wilson MW, Weisburd B, Lek M; Ocular CCDD Phenotyping Consortium; Brand H, Talkowski ME, MacArthur DG, O'Donnell-Luria A, Robson CD, Hunter DG, Engle EC. Jurgens JA, et al. Genet Med. 2025 Apr;27(4):101216. doi: 10.1016/j.gim.2024.101216. Epub 2024 Jul 18. Genet Med. 2025. PMID: 39033378 Free PMC article.

3

Williams syndrome: autosomal dominant inheritance.

Morris CA, Thomas IT, Greenberg F. Morris CA, et al. Among authors: thomas it. Am J Med Genet. 1993 Sep 15;47(4):478-81. doi: 10.1002/ajmg.1320470409. Am J Med Genet. 1993. PMID: 8256809

4

Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation.

Pettenati MJ, Rao N, Johnson C, Hayworth R, Crandall K, Huff O, Thomas IT. Pettenati MJ, et al. Among authors: thomas it. Hum Genet. 1992 Aug;89(6):602-6. doi: 10.1007/BF00221946. Hum Genet. 1992. PMID: 1511976 Review.

5

Transfer-factor treatment in congenital cytomegalovirus infection.

Thomas IT, Soothill JF, Hawkins GT, Marshall WC. Thomas IT, et al. Lancet. 1977 Nov 19;2(8047):1056-7. doi: 10.1016/s0140-6736(77)91887-6. Lancet. 1977. PMID: 72959

6

Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) associated with interstitial deletion of band 3q22: review and gene assignment to the interface of band 3q22.3 and 3q23.

Jewett T, Rao PN, Weaver RG, Stewart W, Thomas IT, Pettenati MJ. Jewett T, et al. Among authors: thomas it. Am J Med Genet. 1993 Dec 1;47(8):1147-50. doi: 10.1002/ajmg.1320470802. Am J Med Genet. 1993. PMID: 8291545 Review.

7

Najjar syndrome revisited.

Thomas IT, Jewett T, Lantz P, Covitz W, Garber P, Berry MN. Thomas IT, et al. Am J Med Genet. 1993 Dec 1;47(8):1151-2. doi: 10.1002/ajmg.1320470803. Am J Med Genet. 1993. PMID: 8291546

8

Teratogens and teratogenesis: general principles of clinical teratology.

Frias JL, Thomas IT. Frias JL, et al. Among authors: thomas it. Ann Clin Lab Sci. 1988 Mar-Apr;18(2):174-9. Ann Clin Lab Sci. 1988. PMID: 3289471 Review.

9

The prospective management of cervicomedullary compression in achondroplasia.

Thomas IT, Frias JL. Thomas IT, et al. Birth Defects Orig Artic Ser. 1989;25(4):83-90. Birth Defects Orig Artic Ser. 1989. PMID: 2697385 Review. No abstract available.

10

Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two cases.

Pettenati MJ, Teot LA, Smith C, Hayworth R, Thomas IT, Veille JC, Rao PN. Pettenati MJ, et al. Among authors: thomas it. Am J Med Genet. 1993 Feb 1;45(3):365-9. doi: 10.1002/ajmg.1320450317. Am J Med Genet. 1993. PMID: 8434625 Review.

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