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Familial café au lait spots: a variant of neurofibromatosis type 1.
Abeliovich D, Gelman-Kohan Z, Silverstein S, Lerer I, Chemke J, Merin S, Zlotogora J. Abeliovich D, et al. Among authors: chemke j. J Med Genet. 1995 Dec;32(12):985-6. doi: 10.1136/jmg.32.12.985. J Med Genet. 1995. PMID: 8825931 Free PMC article.
Medical genetics in Israel.
Zlotogora J, Chemke J. Zlotogora J, et al. Among authors: chemke j. Eur J Hum Genet. 1995;3(3):147-54. doi: 10.1159/000472290. Eur J Hum Genet. 1995. PMID: 7583040 Review.
Genetic services in Israel.
Chemke J, Zlotogora J. Chemke J, et al. Eur J Hum Genet. 1997;5 Suppl 2:105-11. Eur J Hum Genet. 1997. PMID: 9450205 No abstract available.
Homozygosity for inversion (2)(p12q14).
Gelman-Kohan Z, Rosensaft J, Ben-Cohen RN, Chemke J. Gelman-Kohan Z, et al. Among authors: chemke j. Hum Genet. 1993 Oct;92(4):427. doi: 10.1007/BF01247351. Hum Genet. 1993. PMID: 8225326
Prenatal diagnosis of SLO syndrome.
Gelman-Kohan Z, Chemke J. Gelman-Kohan Z, et al. Among authors: chemke j. Am J Med Genet. 1995 Apr 10;56(3):288. doi: 10.1002/ajmg.1320560311. Am J Med Genet. 1995. PMID: 7632278 No abstract available.
Further delineation of the acrocallosal syndrome.
Gelman-Kohan Z, Antonelli J, Ankori-Cohen H, Adar H, Chemke J. Gelman-Kohan Z, et al. Among authors: chemke j. Eur J Pediatr. 1991 Sep;150(11):797-9. doi: 10.1007/BF02026715. Eur J Pediatr. 1991. PMID: 1659985
Cytogenetic analysis of fetal chondrocytes: a comparative study.
Gelman-Kohan Z, Rosensaft J, Ben-Hur H, Haber A, Chemke J. Gelman-Kohan Z, et al. Among authors: chemke j. Prenat Diagn. 1996 Feb;16(2):165-8. doi: 10.1002/(SICI)1097-0223(199602)16:2<165::AID-PD813>3.0.CO;2-E. Prenat Diagn. 1996. PMID: 8650128
92 results