Whelan DT[au] - Search Results

Year	Number of Results
1968	2
1969	2
1970	2
1973	1
1974	1
1975	1
1976	1
1978	1
1979	2
1980	2
1983	3
1984	1
1987	1
1989	1
1995	1
1996	1
1998	2
1999	2
2001	1
2002	2
2003	1
2004	3
2024	0

1

Mass spectrometry and clinical chemistry.

Hill RE, Whelan DT. Hill RE, et al. Among authors: whelan dt. Clin Chim Acta. 1984 Jun 13;139(3):231-94. doi: 10.1016/0009-8981(84)90274-2. Clin Chim Acta. 1984. PMID: 6378430 Review. No abstract available.

2

The oro-facial-digital syndrome.

Whelan DT, Feldman W, Dost I. Whelan DT, et al. Clin Genet. 1975 Sep;8(3):205-12. doi: 10.1111/j.1399-0004.1975.tb01495.x. Clin Genet. 1975. PMID: 1175324

3

Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader-Willi syndrome: a new case and review of the literature.

Nowaczyk MJ, Zeesman S, Kam A, Taylor SA, Carter RF, Whelan DT. Nowaczyk MJ, et al. Among authors: whelan dt. Am J Med Genet A. 2004 Feb 15;125A(1):73-6. doi: 10.1002/ajmg.a.20458. Am J Med Genet A. 2004. PMID: 14755470 Review.

4

Smith-Lemli-Opitz syndrome: a treatable inherited error of metabolism causing mental retardation.

Nowaczyk MJ, Whelan DT, Heshka TW, Hill RE. Nowaczyk MJ, et al. Among authors: whelan dt. CMAJ. 1999 Jul 27;161(2):165-70. CMAJ. 1999. PMID: 10439827 Free PMC article. Review.

5

Paternal transmission of the congenital form of myotonic dystrophy type 1: a new case and review of the literature.

Zeesman S, Carson N, Whelan DT. Zeesman S, et al. Among authors: whelan dt. Am J Med Genet. 2002 Jan 22;107(3):222-6. doi: 10.1002/ajmg.10141. Am J Med Genet. 2002. PMID: 11807903 Review.

6

Citrullinemia: phenotypic variations.

Whelan DT, Brusso T, Spate M. Whelan DT, et al. Pediatrics. 1976 Jun;57(6):935-41. Pediatrics. 1976. PMID: 934749

7

Maternal hyperprolinaemia.

Whelan DT, Conner WT. Whelan DT, et al. Lancet. 1980 Nov 1;2(8201):981-2. doi: 10.1016/s0140-6736(80)92142-x. Lancet. 1980. PMID: 6107623 No abstract available.

8

45,X/46,XX mosaicism in discordant monozygotic twins.

Uchida IA, deSa DJ, Whelan DT. Uchida IA, et al. Among authors: whelan dt. Pediatrics. 1983 Mar;71(3):413-7. Pediatrics. 1983. PMID: 6572357

9

Paternal transmission of fragile X syndrome.

Zeesman S, Zwaigenbaum L, Whelan DT, Hagerman RJ, Tassone F, Taylor SA. Zeesman S, et al. Among authors: whelan dt. Am J Med Genet A. 2004 Aug 30;129A(2):184-9. doi: 10.1002/ajmg.a.30191. Am J Med Genet A. 2004. PMID: 15316964

10

Comparison of urinary acylglycines and acylcarnitines as diagnostic markers of medium-chain acyl-CoA dehydrogenase deficiency.

Rinaldo P, O'Shea JJ, Goodman SI, Miller LV, Fennessey PV, Whelan DT, Hill RE, Tanaka K. Rinaldo P, et al. Among authors: whelan dt. J Inherit Metab Dis. 1989;12 Suppl 2:325-8. doi: 10.1007/BF03335412. J Inherit Metab Dis. 1989. PMID: 2512435 No abstract available.

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