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VANCE MALONEY, M.D.
M.D.
Family Medicine Physician
NPI: 1801823281Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
24866(FL)
Research & Publications (20)
Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficulties.
PMID 18716609·Eur J Hum Genet·2009
5-case
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
PMID 19372089·J Med Genet·2009
8-other
Inverted duplication of 1q32.1 to 1q44 characterized by array CGH and review of distal 1q partial trisomy.
PMID 19248177·Am J Med Genet A·2009
5-case
15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q.
PMID 19133692·Am J Med Genet A·2009
8-other
Distal monosomy 1p36: an atypical case with duodenal atresia and a small interstitial deletion.
PMID 19641456·Clin Dysmorphol·2009
5-case
Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4).
PMID 19104840·Hum Genet·2009
5-case
A complex medical phenotype in a patient with triplication of 2q12.3 to 2q13 characterized with oligonucleotide array CGH.
PMID 19420931·Cytogenet Genome Res·2009
5-case
N-methylpyridoxamine: novel canine vitamin B6 urine metabolite.
PMID 18295484·Bioorg Med Chem Lett·2008
7-preclinical
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
PMID 18784092·N Engl J Med·2008
8-other
Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development.
PMID 18523453·Eur J Hum Genet·2008
5-case
Investigation of the origins of human autosomal inversions.
PMID 18470537·Hum Genet·2008
4-observational
Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.
PMID 18371933·Am J Hum Genet·2008
4-observational
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
PMID 17940555·Eur J Hum Genet·2008
5-case
Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences.
PMID 17318843·Am J Med Genet A·2007
5-case
Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect.
PMID 16954678·Cytogenet Genome Res·2006
5-case
Characterization of SHOX deletions in Leri-Weill dyschondrosteosis (LWD) reveals genetic heterogeneity and no recombination hotspots.
PMID 16826534·Am J Hum Genet·2006
8-other
A highly complex rea(2;3;11) and aniridia by position effect.
PMID 16717455·Cytogenet Genome Res·2006
5-case
Deletions of 2q14 that include the homeobox engrailed 1 (EN1) transcription factor are compatible with a normal phenotype.
PMID 16552425·Eur J Hum Genet·2006
8-other
Molecular investigation of a dicentric 13;17 chromosome found in a 21-week gestation fetus with multiple congenital abnormalities.
PMID 16276107·Cytogenet Genome Res·2006
5-case
A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis.
PMID 16175500·Am J Hum Genet·2005
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
- 540 SABAL LAKE DR APT 106
LONGWOOD, FL 32779 - Phone
- (407) 701-0012
Quick Facts
- NPI
- 1801823281
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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