Fernhoff PM - Search Results

1

Barriers to successful dietary control among pregnant women with phenylketonuria.

Brown AS, Fernhoff PM, Waisbren SE, Frazier DM, Singh R, Rohr F, Morris JM, Kenneson A, MacDonald P, Gwinn M, Honein M, Rasmussen SA. Brown AS, et al. Among authors: fernhoff pm. Genet Med. 2002 Mar-Apr;4(2):84-9. doi: 10.1097/00125817-200203000-00006. Genet Med. 2002. PMID: 11882785 Free article.

2

Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency.

Scaglia F, Wang Y, Singh RH, Dembure PP, Pasquali M, Fernhoff PM, Longo N. Scaglia F, et al. Among authors: fernhoff pm. Genet Med. 1998 Nov-Dec;1(1):34-9. doi: 10.1097/00125817-199811000-00008. Genet Med. 1998. PMID: 11261427 Free article.

3

Maternal and neonatal vitamin B12 deficiency detected through expanded newborn screening--United States, 2003-2007.

Hinton CF, Ojodu JA, Fernhoff PM, Rasmussen SA, Scanlon KS, Hannon WH. Hinton CF, et al. Among authors: fernhoff pm. J Pediatr. 2010 Jul;157(1):162-3. doi: 10.1016/j.jpeds.2010.03.006. Epub 2010 Apr 18. J Pediatr. 2010. PMID: 20400092

4

Vitamin B12 deficiency in children and adolescents.

Rasmussen SA, Fernhoff PM, Scanlon KS. Rasmussen SA, et al. Among authors: fernhoff pm. J Pediatr. 2001 Jan;138(1):10-7. doi: 10.1067/mpd.2001.112160. J Pediatr. 2001. PMID: 11148506 Review. No abstract available.

5

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.

Botto LD, May K, Fernhoff PM, Correa A, Coleman K, Rasmussen SA, Merritt RK, O'Leary LA, Wong LY, Elixson EM, Mahle WT, Campbell RM. Botto LD, et al. Among authors: fernhoff pm. Pediatrics. 2003 Jul;112(1 Pt 1):101-7. doi: 10.1542/peds.112.1.101. Pediatrics. 2003. PMID: 12837874

6

Galactosemia: a strategy to identify new biochemical phenotypes and molecular genotypes.

Elsas LJ, Langley S, Steele E, Evinger J, Fridovich-Keil JL, Brown A, Singh R, Fernhoff P, Hjelm LN, Dembure PP. Elsas LJ, et al. Am J Hum Genet. 1995 Mar;56(3):630-9. Am J Hum Genet. 1995. PMID: 7887416 Free PMC article.

7

Medium chain acyl-CoA dehydrogenase deficiency human genome epidemiology review.

Wang SS, Fernhoff PM, Hannon WH, Khoury MJ. Wang SS, et al. Among authors: fernhoff pm. Genet Med. 1999 Nov-Dec;1(7):332-9. doi: 10.1097/00125817-199911000-00004. Genet Med. 1999. PMID: 11263545 Free article.

8

Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992.

Roberts HE, Moore CA, Fernhoff PM, Brown AL, Khoury MJ. Roberts HE, et al. Among authors: fernhoff pm. Am J Med Genet. 1997 Jul 11;71(1):29-32. doi: 10.1002/(sici)1096-8628(19970711)71:1<29::aid-ajmg5>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9215764

9

Unique mosaicism of tetraploidy and trisomy 8: clinical, cytogenetic, and molecular findings in a live-born infant.

Roberts HE, Saxe DF, Muralidharan K, Coleman KB, Zacharias JF, Fernhoff PM. Roberts HE, et al. Among authors: fernhoff pm. Am J Med Genet. 1996 Mar 29;62(3):243-6. doi: 10.1002/(SICI)1096-8628(19960329)62:3<243::AID-AJMG8>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8882781

10

Creating genetics-based infusion centers: a case study of two models.

Laney DJ, White AL, Rhead WJ, Fernhoff P. Laney DJ, et al. Genet Med. 2008 Aug;10(8):626-32. doi: 10.1097/gim.0b013e31818050a2. Genet Med. 2008. PMID: 18641514

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