Characterization of a human gene encoding nucleosomal binding protein NSBP1KING, Lynn Mertens; FRANCOMANO, Clair A.Genomics (San Diego, Calif.). 2001, Vol 71, Num 2, pp 163-173, issn 0888-7543Article

Latest developments in skeletal dysplasiaHO, Nicola C; FRANCOMANO, Clair A.American journal of medical genetics. 2001, Vol 106, Num 4, issn 0148-7299, 55 p.Serial Issue

Medical genetic studies in the AmishFRANCOMANO, Clair A; BIESECKER, Leslie G.American journal of medical genetics. 2003, Vol 121C, Num 1, issn 0148-7299, 85 p.Serial Issue

The major mutation in the RMRP gene causing CHH among the Amish is the same as that found in most finnish casesRIDANPÄÄ, Maaret; JAIN, Pawan; MCKUSICK, Victor A et al.American journal of medical genetics. 2003, Vol 121C, Num 1, pp 81-83, issn 0148-7299, 3 p.Article

Comprehensive resource: Skeletal Gene DatabaseLIBIN JIA; HO, Nicola C; PARK, Susan S et al.American journal of medical genetics. 2001, Vol 106, Num 4, pp 275-281, issn 0148-7299Article

Genetic heritage of the Old Order Mennonites of southeastern PennsylvaniaPUFFENBERGER, E. G.American journal of medical genetics. 2003, Vol 121C, Num 1, pp 18-31, issn 0148-7299, 14 p.Article

Transcriptional dysregulation in skeletal malformation syndromesHERMANNS, Pia; LEE, Brendan.American journal of medical genetics. 2001, Vol 106, Num 4, pp 258-271, issn 0148-7299Article

Anabaptist Genealogy DatabaseAGARWALA, Richa; BIESECKER, Leslie G; SCHÄFFER, Alejandro A et al.American journal of medical genetics. 2003, Vol 121C, Num 1, pp 32-37, issn 0148-7299, 6 p.Article

Type I glutaric aciduria, Part 2: A model of acute striatal necrosisSTRAUSS, Kevin A; MORTON, D. Holmes.American journal of medical genetics. 2003, Vol 121C, Num 1, pp 53-70, issn 0148-7299, 18 p.Article

Allelic and nonallelic heterogeneity in dyschondrosteosis (Leri-Weill syndrome)CORMIER-DAIRE, Valerie; HUBER, Céline; MUNNICH, Arnold et al.American journal of medical genetics. 2001, Vol 106, Num 4, pp 272-274, issn 0148-7299Article

A Skeletal Gene DatabaseHO, Nicola C; LIBIN JIA; DRISCOLL, Catherine C et al.Journal of bone and mineral research (Print). 2000, Vol 15, Num 11, pp 2095-2122, issn 0884-0431Article

The influence of pulsed low-intensity ultrasound on matrix production of chondrocytes at different stages of differentiation: An explant studyZHANG, Zi-Jun; HUCKLE, James; FRANCOMANO, Clair A et al.Ultrasound in medicine & biology. 2002, Vol 28, Num 11-12, pp 1547-1553, issn 0301-5629, 7 p.Article

Case 47HO, Nicola C; HADLEY, Donald W; JAIN, Pawan K et al.Radiology. 2002, Vol 222, Num 2, pp 513-514, issn 0033-8419Article

Syndrome of occipitoatlantoaxial hypermobility, cranial settling, and Chiari malformation Type I in patients with hereditary disorders of connective tissueMILHORAT, Thomas H; BOLOGNESE, Paolo A; NISHIKAWA, Misao et al.Journal of neurosurgery. Spine. 2007, Vol 7, Num 6, pp 601-609, issn 1547-5654, 9 p.Article

Dyssegmental dysplasia, Silverman-Handmaker type: Unexpected role of perlecan in cartilage developmentARIKAWA-HIRASAWA, Eri; WILCOX, William R; YAMADA, Yoshihiko et al.American journal of medical genetics. 2001, Vol 106, Num 4, pp 254-257, issn 0148-7299Article

Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf miceIWATA, Tomoko; LI, Cui-Ling; DENG, Chu-Xia et al.Human molecular genetics (Print). 2001, Vol 10, Num 12, pp 1255-1264, issn 0964-6906Article

Pseudoachondroplasia and multiple epiphyseal dysplasia: New etiologic developmentsUNGER, Sheila; HECHT, Jacqueline T.American journal of medical genetics. 2001, Vol 106, Num 4, pp 244-250, issn 0148-7299Article

Molecular-pathogenetic Classification of genetic disorders of the skeletonSUPERTI-FURGA, Andrea; BONAFE, Luisa; RIMOIN, David L et al.American journal of medical genetics. 2001, Vol 106, Num 4, pp 282-289, issn 0148-7299Article

The effects of pulsed low-intensity ultrasound on chondrocyte viability, proliferation, gene expression and matrix productionZHANG, Zi-Jun; HUCKLE, James; FRANCOMANO, Clair A et al.Ultrasound in medicine & biology. 2003, Vol 29, Num 11, pp 1645-1651, issn 0301-5629, 7 p.Article

Case 47: Dural ectasia associated with Marfan syndromeHO, Nicola C; HADLEY, Donald W; JAIN, Pawan K et al.Radiology. 2002, Vol 223, Num 3, pp 767-771, issn 0033-8419Article

Type I glutaric aciduria, Part 1: Natural history of 77 patientsSTRAUSS, Kevin A; PUFFENBERGER, Erik G; ROBINSON, Donna L et al.American journal of medical genetics. 2003, Vol 121C, Num 1, pp 38-52, issn 0148-7299, 15 p.Article

Gene expression profile of human bone marrow stromal cells: High-throughput expressed sequence tag sequencing analysisJIA, Libin; YOUNG, Marian F; POWELL, John et al.Genomics (San Diego, Calif.). 2002, Vol 79, Num 1, pp 7-17, issn 0888-7543Article

Issues surrounding prenatal genetic testing for achondroplasiaGOODING, Holly C; BOEHM, Karina; THOMPSON, Richard E et al.Prenatal diagnosis. 2002, Vol 22, Num 10, pp 933-940, issn 0197-3851Article

Association of Chiari malformation type I and tethered cord syndrome: preliminary results of sectioning filum terminaleMILHORAT, Thomas H; BOLOGNESE, Paolo A; NISHIKAWA, Misao et al.Surgical neurology. 2009, Vol 72, Num 1, pp 20-35, issn 0090-3019, 16 p.Article

A central nervous system specific mouse model for thanatophoric dysplasia type IITI LIN; SANDUSKY, Stacey B; HAIPENG XUE et al.Human molecular genetics (Print). 2003, Vol 12, Num 21, pp 2863-2871, issn 0964-6906, 9 p.Article