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MCCALL ZENKER, PHARMD
PHARMD
Pharmacist
NPI: 1396295333Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
RPH5233(ND)
Research & Publications (20)
Severe, neonatal-onset OTC deficiency in twin sisters with a de novo balanced reciprocal translocation t(X;5)(p21.1;q11).
PMID 15578616·Am J Med Genet A·2005
5-case
Application of ultrasound-assisted thermal processing for preservation and quality retention of liquid foods.
PMID 14503719·J Food Prot·2003
8-other
Monosomy 1p36--a recently delineated, clinically recognizable syndrome.
PMID 11822705·Clin Dysmorphol·2002
5-case
Paravertebral and intraspinal malposition of transfemoral central venous catheters in newborns.
PMID 10839887·J Pediatr·2000
5-case
A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.
PMID 19225462·Eur J Hum Genet·2009
8-other
Genetics of nephrotic syndrome: new insights into molecules acting at the glomerular filtration barrier.
PMID 19649571·J Mol Med (Berl)·2009
6-review
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.
PMID 19264732·J Med Genet·2009
8-other
Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap.
PMID 19277062·Eur J Hum Genet·2009
8-other
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects.
PMID 19610107·Am J Med Genet A·2009
5-case
Oculopharyngeal muscular dystrophy as a rare differential diagnosis for unexplained dysphagia: a case report.
PMID 19175930·Cases J·2009
8-other
Infantile hypophosphatasia due to a new compound heterozygous TNSALP mutation - functional evidence for a hydrophobic side-chain?
PMID 18523927·Exp Clin Endocrinol Diabetes·2009
5-case
SMARCAL1 mutations: a cause of prepubertal idiopathic steroid-resistant nephrotic syndrome.
PMID 19127206·Pediatr Res·2009
5-case
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome.
PMID 18854871·Eur J Hum Genet·2009
8-other
Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations.
PMID 19396835·Am J Med Genet A·2009
5-case
Independent NF1 and PTPN11 mutations in a family with neurofibromatosis-Noonan syndrome.
PMID 19449407·Am J Med Genet A·2009
5-case
Local clustering of PRSS1 R122H mutations in hereditary pancreatitis patients from Northern Germany.
PMID 18702646·Am J Gastroenterol·2008
4-observational
Johanson-Blizzard syndrome caused by identical UBR1 mutations in two unrelated girls, one with a cardiomyopathy.
PMID 19006206·Am J Med Genet A·2008
5-case
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2807 PLAINVIEW DR SE
MANDAN, ND 58554 - Phone
- (701) 290-6441
Quick Facts
- NPI
- 1396295333
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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