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American Journal of Medical Genetics, ISSN 0148-7299, 01/1989, Volume 32, Issue 1, pp. 36 - 41
Journal Article
by Gatsonis, Constantine A and Aberle, Denise R and Berg, Christine D and Black, William C and Church, Timothy R and Fagerstrom, Richard M and Galen, Barbara and Gareen, Ilana F and Goldin, Jonathan and Gohagan, John K and Hillman, Bruce and Jaffe, Carl and Kramer, Barnett S and Lynch, David and Marcus, Pamela M and Schnall, Mitchell and Sullivan, Daniel C and Sullivan, Dorothy and Zylak, Carl J and Cagnon, Christopher and Cody, Dianna and Fletcher, Glenn and Flynn, Michael J and Judy, Philip F and Kruger, Randell and Larke, Frederick J and McNitt-Gray, Michael and Payne, Thomas and Anthony Seibert, J and Wu, Xizeng and Abbott, Gerald and Amorosa, Judith K and Barr, Richard G and Boiselle, Phillip M and Chiles, Caroline and Clark, Robert and Coppage, Lynn and Falk, Robert and Fishman, Elliot K and Gemmel, David and Goldin, Jonathan G and Goodman, Eric and Hart, Eric M and Hazelton, Todd and Johnson, Elizabeth and Kazerooni, Ella and McComb, Barbara and McLennan, Geoffrey and Munden, Reginald F and Ravenel, James and Sullivan, Michael and Swensen, Stephen J and Torigian, Drew A and Vydareny, Kay H and Worrell, John A and Balkin, Peter and Fouad, Mona and Freedman, Matthew T and Garg, Kavita and Gelmann, Edward P and Gierada, David S and Hocking, William and Inampudi, Subbarao and Isaacs, Claudine and Kvale, Paul and Mann, Howard and Manor, William and Nath, Hrudaya and Reding, Douglas and Spizarny, David L and Strollo, Diane C and Waltz, John and Chen, Mei-Hsiu and Duan, Fenghai and Izmirilian, Grant and Pinsky, Paul and Prorok, Philip C and Miller, Anthony B and Edelman, Martin J and Evans, William K and Fontana, Robert S and Machtay, Mitchell and Clark, Kenneth W and Clingan, Kathy L and Ford, Melissa B and Márquez, Guillermo and Moore, Steven M and Ohan, Peter and Payne, Thomas J and Peace, Steven and Rosenbaum, Jennifer L and Barr, Richard and Black, William and Torigian, Drew and Vydareny, Kay and Worrell, John and Young, Robert C and Alberts, David and DeMets, David and Greenwald, Peter and ... and Natl Lung Screening Trial Res Team and National Lung Screening Trial Research Team
Radiology, ISSN 0033-8419, 01/2011, Volume 258, Issue 1, pp. 243 - 253
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 04/2007, Volume 44, Issue 4, pp. 264 - 268
This report presents the detection of a heterozygous deletion at chromosome 12q14 in three unrelated patients with a similar phenotype consisting of mild... 
GRIP1 | GENE | LIPOMAS | ARRAY-CGH | GENETICS & HEREDITY | FACTOR HMGI-C | COMPARATIVE GENOMIC HYBRIDIZATION | MESENCHYMAL TUMORS | REARRANGEMENTS | PROTEINS | PULMONARY CHONDROID HAMARTOMAS | Sequence Deletion | Scoliosis - genetics | Oligonucleotide Array Sequence Analysis | Humans | Failure to Thrive - etiology | Infant | Male | HMGA2 Protein - physiology | Intellectual Disability - genetics | Chromosomes, Human, Pair 12 - ultrastructure | Membrane Proteins - deficiency | Nuclear Proteins - deficiency | Chromosomes, Artificial, Bacterial | HMGA2 Protein - genetics | Adult | Female | Nuclear Proteins - genetics | Chromosomes, Human, Pair 12 - genetics | Abnormalities, Multiple - genetics | Chromosome Breakage | Infant, Newborn | Carrier Proteins - physiology | Chromosome Deletion | Infant, Low Birth Weight | Chromosome Disorders - pathology | Nerve Tissue Proteins - physiology | Membrane Proteins - genetics | Chromosome Mapping | Nerve Tissue Proteins - genetics | Syndrome | Carrier Proteins - genetics | Dwarfism - genetics | Osteopoikilosis - genetics | Phenotype | Heterozygote | Learning Disorders - genetics | Chromosome Disorders - genetics | Case studies | Musculoskeletal diseases | Chromosome deletion | Genetic aspects | Stature, Short | Mental retardation | Pregnancy | Hypertension | Genotype & phenotype | Scoliosis | Intellectual disabilities | Growth hormones | Gene expression | Patients | Age | Tumors | mental retardation | short stature | HMGA2 | Short Report | osteopoikilosis
Journal Article