Showing results (531-540 of 8,534) with videos related to
Sort By:
Pageof 854
American Journal of Medical Genetics|May 8, 1999
Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type IIP Mandich, E Bellone, E Di Maria, et al.American Journal of Medical Genetics|May 8, 1999
X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: linkage study and neuropsychological data in a large familyC Gendrot, N Ronce, M Raynaud, et al.American Journal of Medical Genetics|April 24, 1999
Craniosynostosis associated with ectopia lentis in monozygotic twin sistersJ R Cruysberg, C M van Ravenswaaij-Arts, A Pinckers, et al.American Journal of Medical Genetics|April 24, 1999
Uniparental isodisomy resulting from 46,XX,i(1p),i(1q) in a woman with short stature, ptosis, micro/retrognathia, myopathy, deafness, and sterilityH Chen, R Young, X Mu, et al.American Journal of Medical Genetics|April 24, 1999
Thumb/hallux duplication and preaxial polydactyly type II M Orioli, E E CastillaAmerican Journal of Medical Genetics|April 24, 1999
Lethal neonatal Hutchinson-Gilford progeria syndromeJ I Rodríguez, P Pérez-Alonso, R Funes, et al.American Journal of Medical Genetics|March 30, 1999
Commercialization of BRCA1/2 testing: practitioner awareness and use of a new genetic testM K Cho, P Sankar, P R Wolpe, et al.American Journal of Medical Genetics|March 30, 1999
Synteny-defined candidate genes for congenital and idiopathic scoliosisP F Giampietro, C L Raggio, R D BlankAmerican Journal of Medical Genetics|March 30, 1999
Complex camptopolydactyly: an unusual hand malformationS R Phadke, P GautamAmerican Journal of Medical Genetics|April 17, 1999
No evidence for linkage between schizophrenia and markers at chromosome 15q13-14L Curtis, J L Blouin, U Radhakrishna, et al.Pageof 854