A comprehensive review of reported heritable noggin-associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term: NOG-related-symphalangism spectrum disorder (NOG-SSD)

Signaling Pathways in Human Skeletal Dysplasias

(2010) Dustin Baldridge et al.   Annual Review of Genomics and Human Genetics

Dominant inheritance of multiple epiphyseal dysplasia, myopia and deafness

(2010) P. Beighton et al.   CLINICAL GENETICS

The facio-audio-symphalangism syndrome: report of a case and review of the literature

(2010) S. A. Hurvitz et al.   CLINICAL GENETICS

Congenital malformation of the feet with low body height

(2010) Hans N. Gregersen et al.   CLINICAL GENETICS

Extracellular regulation of BMP signaling

(2010) Lise Zakin et al.   CURRENT BIOLOGY

Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene

(2009) Xiao-lin Wu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Identification and association analysis of single nucleotide polymorphisms in the human noggin (NOG) gene and osteoporosis phenotypes

(2009) Susan P. Moffett et al.   BONE

High-Density Association Study of 383 Candidate Genes for Volumetric BMD at the Femoral Neck and Lumbar Spine Among Older Men

(2009) Laura M Yerges et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

(2009) Elisabeth Mangold et al.   NATURE GENETICS

Otosclerosis or Congenital Stapes Ankylosis? The Diagnostic Role of Genetic Analysis

(2009) Sarah B. Emery et al.   OTOLOGY & NEUROTOLOGY

P35S mutation in the NOG gene associated with Teunissen–Cremers syndrome and features of multiple NOG joint-fusion syndromes

(2008) Nir Hirshoren et al.   European Journal of Medical Genetics

Growth and Skeletal Development in Families with NOGGIN Gene Mutations

(2008) C.D. Oxley et al.   Hormone Research in Paediatrics

Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangism

(2008) Wei Yang et al.   JOURNAL OF HUMAN GENETICS

Many sequence variants affecting diversity of adult human height

(2008) Daniel F Gudbjartsson et al.   NATURE GENETICS