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Nucleic Acids Research|June 19, 2001
Identification and prevention of a GC content bias in SAGE librariesE H Margulies, S L Kardia, J W InnisNature Genetics|July 1, 1996
The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formationD P Mortlock, L C Post, J W InnisGenome Research|April 1, 1996
An efficient method for isolating putative promoters and 5'-transcribed sequences from large genomic clonesD P Mortlock, M R Nelson, J W InnisGenome Research|October 10, 2001
A comparative molecular analysis of developing mouse forelimbs and hindlimbs using serial analysis of gene expression (SAGE)E H Margulies, S L Kardia, J W InnisAmerican Journal of Medical Genetics|February 5, 1998
Apparently new syndrome of sensorineural hearing loss, retinal pigment epithelium lesions, and discolored teethJ W Innis, P A Sieving, P McMillan, et al.Developmental Biology|January 8, 2000
Severe limb defects in Hypodactyly mice result from the expression of a novel, mutant HOXA13 proteinL C Post, E H Margulies, A Kuo, et al.American Journal of Medical Genetics|August 8, 1997
Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomaliesJ W Innis, J H Asher, A K Poznanski, et al.American Journal of Human Genetics|June 30, 2001
A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes diseaseS L Dagenais, A N Adam, J W Innis, et al.Journal of Medical Genetics|April 16, 1998
Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7M L Carey, T B Friedman, J H Asher, et al.Human Genetics|September 1, 1995
Two highly polymorphic CA repeats in the Menkes gene (ATP7A)C R Begy, H A Dierick, J W Innis, et al.Pageof 3