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REID LACHMAN, MD
MD
Otolaryngology Physician
NPI: 1336174614Individual
Specialties, Licenses & Credentials
Otolaryngology PhysicianPrimary
Otolaryngology
Code: 207Y00000X
MA047239(NJ)
Research & Publications (20)
The Erlenmeyer flask bone deformity in the skeletal dysplasias.
PMID 19444897·Am J Med Genet A·2009
6-review
A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C-type lectin domain of aggrecan.
PMID 19110214·Am J Hum Genet·2009
8-other
Mutations in the gene encoding the calcium-permeable ion channel TRPV4 produce spondylometaphyseal dysplasia, Kozlowski type and metatropic dysplasia.
PMID 19232556·Am J Hum Genet·2009
8-other
Guidelines for the prenatal diagnosis of fetal skeletal dysplasias.
PMID 19265753·Genet Med·2009
7-preclinical
A phenotype intermediate between Desbuquois dysplasia and diastrophic dysplasia secondary to mutations in DTDST.
PMID 18925670·Am J Med Genet A·2008
5-case
Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: a retrospective and prospective analysis.
PMID 18627037·Am J Med Genet A·2008
8-other
De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.
PMID 18203189·Am J Med Genet A·2008
5-case
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia.
PMID 18587396·Nat Genet·2008
8-other
Molecular characterization of a patient with an interstitial 1q deletion [del(1)(q24.1q25.3)] and distinctive skeletal abnormalities.
PMID 18925675·Am J Med Genet A·2008
5-case
The impact of the 2004 tsunami on coastal Thai communities: assessing adaptive capacity.
PMID 18217920·Disasters·2008
8-other
Multilayered patella: similar radiographic findings in pseudoachondroplasia and recessive multiple epiphyseal dysplasia.
PMID 18546327·Am J Med Genet A·2008
5-case
Van den Ende-Gupta syndrome: laryngeal abnormalities in two siblings.
PMID 17937442·Am J Med Genet A·2007
5-case
The skeletal dysplasias: clinical-molecular correlations.
PMID 18056050·Ann N Y Acad Sci·2007
6-review
Diaphanospondylodysostosis: six new cases and exclusion of the candidate genes, PAX1 and MEOX1.
PMID 17764081·Am J Med Genet A·2007
5-case
The Shwachman-Bodian-Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian type.
PMID 17400792·J Med Genet·2007
5-case
Angulated femurs and the skeletal dysplasias: experience of the International Skeletal Dysplasia Registry (1988-2006).
PMID 17486589·Am J Med Genet A·2007
8-other
A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.
PMID 16801345·J Med Genet·2007
8-other
Mutations in two regions of FLNB result in atelosteogenesis I and III.
PMID 16752402·Hum Mutat·2006
8-other
Osteocraniostenosis-hypomineralized skull with gracile long bones and splenic hypoplasia. Four new cases with distinctive chondro-osseous morphology.
PMID 16770805·Am J Med Genet A·2006
5-case
Terminal phalangeal accessory ossification center of the thumb: an additional radiographic finding in Larsen syndrome.
PMID 16715218·Pediatr Radiol·2006
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 95 MADISON AVE, STE 105
MORRISTOWN, NJ 07960 - Phone
- (973) 644-0808
Quick Facts
- NPI
- 1336174614
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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