au.\*:("GARBER, A. P")
Results 1 to 6 of 6
Selection :
Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentrometric region of chromosome 19BRIGGS, M. D; RASMUSSEN, M; WEBER, J. L et al.Genomics (San Diego, Calif.). 1993, Vol 18, Num 3, pp 656-660, issn 0888-7543Article
A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia : exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrixRIMOIN, D. L; RASMUSSEN, I. M; GARBER, A. P et al.Human genetics. 1994, Vol 93, Num 3, pp 236-242, issn 0340-6717Article
osteogenesis imperfecta type III. Delineation of the phenotype with reference to genetic heterogeneitySILLENCE, D. O; BARLOW, K. K; COLE, W. G et al.American journal of medical genetics. 1986, Vol 23, Num 3, pp 821-832, issn 0148-7299Article
Mosaic trisomy 16 ascertained through amniocentesis : Evaluation of 11 new casesHSU, W.-T; SHCHEPIN, D. A; HAJIANPOUR, M. J et al.American journal of medical genetics. 1998, Vol 80, Num 5, pp 473-480, issn 0148-7299Article
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome I containing a type IX collagen geneBRIGGS, M. D; HICHANG CHOI; BIESECKER, L. G et al.American journal of human genetics. 1994, Vol 55, Num 4, pp 678-684, issn 0002-9297Article
Prenatal genetic counselingGARBER, A. P; HIXON, H. E. C.Clinics in perinatology. 1990, Vol 17, Num 4, pp 749-759, issn 0095-5108, 11 p.Article