McLeod DR - Search Results

1

Acute hemorrhagic leukoencephalitis in male sibs.

McLeod DR, Snyder F, Bridge P, Pinto A. McLeod DR, et al. Am J Med Genet. 2002 Feb 1;107(4):325-9. doi: 10.1002/ajmg.10169. Am J Med Genet. 2002. PMID: 11840490

2

Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition.

Davey KM, Parboosingh JS, McLeod DR, Chan A, Casey R, Ferreira P, Snyder FF, Bridge PJ, Bernier FP. Davey KM, et al. Among authors: mcleod dr. J Med Genet. 2006 May;43(5):385-93. doi: 10.1136/jmg.2005.036657. Epub 2005 Jul 31. J Med Genet. 2006. PMID: 16055927 Free PMC article.

3

A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch-German) Mennonite and Hutterite patients in North America.

Loucks C, Parboosingh JS, Chong JX, Ober C, Siu VM, Hegele RA, Rupar CA, McLeod DR, Pinto A, Chudley AE, Innes AM. Loucks C, et al. Among authors: mcleod dr. Am J Med Genet A. 2012 May;158A(5):1229-32. doi: 10.1002/ajmg.a.35302. Epub 2012 Apr 11. Am J Med Genet A. 2012. PMID: 22495976 Free PMC article. No abstract available.

4

Deficiency of 5-oxoprolinase in an 8-year-old with developmental delay.

Bernier FP, Snyder FF, McLeod DR. Bernier FP, et al. Among authors: mcleod dr. J Inherit Metab Dis. 1996;19(3):367-8. doi: 10.1007/BF01799269. J Inherit Metab Dis. 1996. PMID: 8803782 No abstract available.

5

Dihydropyrimidine dehydrogenase deficiency in a Hutterite newborn.

Adolph KJ, Fung E, McLeod DR, Morgan K, Snyder FF. Adolph KJ, et al. Among authors: mcleod dr. Adv Exp Med Biol. 1991;309B:311-4. doi: 10.1007/978-1-4615-7703-4_69. Adv Exp Med Biol. 1991. PMID: 1781388 No abstract available.

6

A new variant of lethal neonatal short-limbed platyspondylic dwarfism.

Pinto A, Hwang WS, McLeod DR, Moscowitz W, Lachman RS, Rimoin DL. Pinto A, et al. Among authors: mcleod dr. Arch Pathol Lab Med. 1993 Mar;117(3):322-5. Arch Pathol Lab Med. 1993. PMID: 8442677

7

VACTERL manifestations in two generations of a family.

Nezarati MM, McLeod DR. Nezarati MM, et al. Among authors: mcleod dr. Am J Med Genet. 1999 Jan 1;82(1):40-2. Am J Med Genet. 1999. PMID: 9916841

8

Combination of renal agenesis with respiratory and alimentary tract atresia results in normal lung development.

McLeod DR, Akierman A, Trevenen C. McLeod DR, et al. Am J Med Genet. 2001 Sep 1;102(4):327-9. doi: 10.1002/ajmg.1485. Am J Med Genet. 2001. PMID: 11503159

9

Autosomal dominant flat umbilicus.

Leung AK, McLeod DR. Leung AK, et al. Among authors: mcleod dr. Am J Med Genet A. 2004 Dec 15;131(3):307-9. doi: 10.1002/ajmg.a.30395. Am J Med Genet A. 2004. PMID: 15523632

10

Metacarpophalangeal pattern profile analysis in Williams syndrome.

Burns MA, McLeod DR, Linton LR, Butler MG. Burns MA, et al. Among authors: mcleod dr. Am J Med Genet. 1993 Sep 15;47(4):471-4. doi: 10.1002/ajmg.1320470407. Am J Med Genet. 1993. PMID: 8256807 Free PMC article.

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