Chemke J - Search Results

1

Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.

Chemke J, Carmi R, Galil A, Bar-Ziv Y, Ben-Ytzhak I, Zurkowski L. Chemke J, et al. Am J Med Genet. 1992 Aug 1;43(6):989-95. doi: 10.1002/ajmg.1320430616. Am J Med Genet. 1992. PMID: 1415350 Review.

2

COL11A2 mutation associated with autosomal recessive Weissenbacher-Zweymuller syndrome: molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED).

Harel T, Rabinowitz R, Hendler N, Galil A, Flusser H, Chemke J, Gradstein L, Lifshitz T, Ofir R, Elbedour K, Birk OS. Harel T, et al. Among authors: chemke j. Am J Med Genet A. 2005 Jan 1;132A(1):33-5. doi: 10.1002/ajmg.a.30371. Am J Med Genet A. 2005. PMID: 15558753

3

Autosomal recessive inheritance of Nager acrofacial dysostosis.

Chemke J, Mogilner BM, Ben-Itzhak I, Zurkowski L, Ophir D. Chemke J, et al. J Med Genet. 1988 Apr;25(4):230-2. doi: 10.1136/jmg.25.4.230. J Med Genet. 1988. PMID: 3367347 Free PMC article.

4

Weissenbacher-Zweymuller syndrome: long-term follow-up of growth and psychomotor development.

Galil A, Carmi R, Goldstein E, Porter B, Bar Ziv J, Chemke J. Galil A, et al. Among authors: chemke j. Dev Med Child Neurol. 1991 Dec;33(12):1104-9. doi: 10.1111/j.1469-8749.1991.tb14834.x. Dev Med Child Neurol. 1991. PMID: 1723388

5

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.

6

Trisomy 9 confined to the placenta: prenatal diagnosis and neonatal follow-up.

Appelman Z, Rosensaft J, Chemke J, Caspi B, Ashkenazi M, Mogilner MB. Appelman Z, et al. Among authors: chemke j. Am J Med Genet. 1991 Sep 15;40(4):464-6. doi: 10.1002/ajmg.1320400418. Am J Med Genet. 1991. PMID: 1746612

7

Adrenoleukodystrophy in Israel: a genetic, clinical and biochemical study.

Chemke J, Lieberman E, Carmi R, Abarbanel Y, Costeff H, Goldhammer Y, Moser HW. Chemke J, et al. Isr J Med Sci. 1984 Dec;20(12):1123-32. Isr J Med Sci. 1984. PMID: 6097565

8

Homozygosity for autosomal dominant Marfan syndrome.

Chemke J, Nisani R, Feigl A, Garty R, Cooper M, Bårash Y, Duksin D. Chemke J, et al. J Med Genet. 1984 Jun;21(3):173-7. doi: 10.1136/jmg.21.3.173. J Med Genet. 1984. PMID: 6748012 Free PMC article.

9

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

10

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

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