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

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. 2024 Jul 17:101216. doi: 10.1016/j.gim.2024.101216. Online ahead of print. Genet Med. 2024. PMID: 39033378 Free article.

3

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.

4

Magnetic resonance imaging in the assessment of medullary compression in achondroplasia.

Thomas IT, Frias JL, Williams JL, Friedman WA. Thomas IT, et al. Am J Dis Child. 1988 Sep;142(9):989-92. doi: 10.1001/archpedi.1988.02150090087031. Am J Dis Child. 1988. PMID: 3046333 Review.

5

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

6

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.

7

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.

Thomas IT, Frias JL, Cantu ES, Lafer CZ, Flannery DB, Graham JG Jr. Thomas IT, et al. Am J Hum Genet. 1989 Aug;45(2):193-205. Am J Hum Genet. 1989. PMID: 2667350 Free PMC article. Review.

8

Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation.

Cantú ES, Thomas IT, Frias JL. Cantú ES, et al. Among authors: thomas it. Clin Genet. 1989 Sep;36(3):189-95. doi: 10.1111/j.1399-0004.1989.tb03187.x. Clin Genet. 1989. PMID: 2676269 Review.

9

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.

10

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

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