J. Chemke

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Asymmetry and discordance for congenital anomalies in conjoined twins: a report of six cases.

A. Ornoy, N. Laufer, D. Navot, 1980, Teratology.

Prenatal diagnosis of Meckel syndrome: alpha‐feto protein and beta‐trace protein in amniotic fluid

Z. Katz, J. Chemke, A. Miskin, 1977, Clinical genetics.

Acrocallosal syndrome: identification of a novel KIF7 mutation and evidence for oligogenic inheritance.

M. Simpson, R. Trembath, E. Maher, 2013, European journal of medical genetics.

The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+).

A. Robinson, J. Chemke, Juan CHEMKEt, 1971, Journal of medical genetics.

Epidermal mosaicism and Blaschko's lines.

Miguel Ángel Martínez, Jacques Mallet, R. Meloni, 1994, Journal of medical genetics.

Separation and determination of saturated very-long-chain free fatty acids in plasma of patients with adrenoleukodystrophy using solid-phase extraction and high-performance liquid chromatographic analysis.

E. Grushka, J. Chemke, I. Zamir, 1991, Journal of chromatography.

Adrenoleukodystrophy: evidence for cytoplasmic inclusions in white blood cells.

N. Livni, E. Rosenmann, J. Chemke, 1986, Pediatric pathology.

Adrenoleukodystrophy: Very long‐chain fatty acid metabolism in fibroblasts

W. Rizzo, J. Avigan, J. Schulman, 1984, Neurology.

Familial Recurring Thanatophoric Dwarfism: A Case Report

M. Lancet, J. Chemke, G. Graff, 1972, Obstetrics and gynecology.

Familial thanatophoric dwarfism.

M. Lancet, J. Chemke, G. Graff, 1971, Lancet.

A possible effect of ultrasound on RNA synthesis in cultured amniocytes

E. Shalev, J. Chemke, Y. Shneyour, 1993, Acta obstetricia et gynecologica Scandinavica.

RISING RATES OF CONGENITAL DISLOCATION OF THE HIP

Rina Chen, J. Chemke, M. Klingberg, 1976, The Lancet.

CHROMOSOMAL ABNORMALITIES IN SEZARY'S LYMPHOMA

A. Berrebi, E. Vorst, J. Chemke, 1989, European journal of haematology.

Medical Genetics in Israel

J. Zlotogora, J. Chemke, 1995, European journal of human genetics : EJHG.

Occurrence of hereditary nephritis, pretibial epidermolysis bullosa and beta-thalassemia minor in two siblings with end-stage renal disease.

Y. Bar-Khayim, S. Feld, J. Chemke, 1988, Nephron.

Absence of teratogenicity of indomethacin in ovarian hyperstimulation syndrome.

Z. Katz, M. Lancet, R. Borenstein, 1984, International journal of fertility.

Teratogenicity of Progestogens Given During the First Trimester of Pregnancy

Z. Katz, M. Lancet, B. Mogilner, 1985, Obstetrics and gynecology.

Isolated foveal hypoplasia.

F. Abraham, M. Oliver, J. Chemke, 1987, The British journal of ophthalmology.

The third fontanelle.

J. Chemke, A. Robinson, 1969, The Journal of pediatrics.

Standard Outline for Each Nation (2.1–2.19)

K. E. Tranøy, F. Salzano, L. Bolund, 1989 .

Homozygosity for autosomal dominant Marfan syndrome.

Y. Barash, D. Duksin, J. Chemke, 1984, Journal of medical genetics.

ABSENCE OF CHROMOSOMAL CHANGES IN FETUS AFTER PATERNAL CHEMOTHERAPY

M. Talpaz, A. Shani, J. Chemke, 1979, The Lancet.

Familial XY gonadal dysgenesis.

A. Robinson, J. Chemke, R. Carmichael, 1970, Journal of medical genetics.

Absent ulna in the Klippel‐Feil syndrome: an unusual associated malformation

J. Chemke, R. Nisani, R. Fischel, 1980, Clinical genetics.

Prenatal diagnosis of severe congenital malformations associated with elevated amniotic fluid alpha–feto protein

M. Lancet, N. Hurwitz, J. Chemke, 1979, Clinical genetics.

COL11A2 mutation associated with autosomal recessive Weissenbacher–Zweymuller syndrome: Molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED)

K. Elbedour, R. Ofir, O. Birk, 2005, American journal of medical genetics. Part A.

CYTOGENETIC ANALYSIS OF FETAL CHONDROCYTES: A COMPARATIVE STUDY

H. Ben‐Hur, J. Rosensaft, J. Chemke, 1996, Prenatal diagnosis.

Familial glioblastoma multiforme without neurofibromatosis.

D. Katznelson, J. Chemke, G. Zucker, 1985, American journal of medical genetics.

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

R. Carmi, A. Galil, J. Chemke, 1992, American journal of medical genetics.

Weissenbacher‐Zweymuller Syndrome; Long‐term Follow‐up of Growth and Psychomotor Development

R. Carmi, A. Galil, J. Chemke, 1991, Developmental medicine and child neurology.

Effector T lymphocyte line cells migrate to the thymus and persist there

I. Cohen, A. Ben-nun, Y. Naparstek, 1982, Nature.

Neural tube defects in trisomy 18

F. Nissim, J. Chemke, R. Nisani, 1981, Prenatal diagnosis.

Aberrant melanoblast migration associated with trisomy 18 mosaicism.

J. Chemke, S. Rappaport, R. Etrog, 1983, Journal of medical genetics.

Cytogenetic studies in megakaryoblastic leukaemia.

A. Berrebi, A. Dvilanski, J. Chemke, 1983, Acta haematologica.

The Amniotic Band Syndrome

N. Hurwitz, J. Chemke, E. Liban, 1973, Obstetrics and gynecology.

Homozygosity for inversion (2)(p12q14)

J. Rosensaft, J. Chemke, Z. Gelman-Kohan, 1993, Human Genetics.

A case of infantile Jakob-Creutzfeldt disease

U. Sandbank, J. Chemke, 1965, Acta Neuropathologica.

Maple syrup urine disease. Two cases in Israel.

J. Chemke, S. Levin, 1975, Israel journal of medical sciences.

Multiple skeletal anomalies in the “13q-” syndrome

M. Zalish, E. Fishel, J. Chemke, 1978, European Journal of Pediatrics.

RISING RATES OF CONGENITAL DISLOCATION OF THE HIP?

J. Chemke, M. Klingberg, R. Chen, 1976, The Lancet.

Further delineation of the acrocallosal syndrome

Z. Gelman-Kohan, J. Antonelli, H. Ankori-Cohen, 1991, European Journal of Pediatrics.

Male to male transmission of the G syndrome

J. Chemke, H. Ankori-Cohen, E. Shor, 1984, Clinical genetics.

Amniocentesis rate and the detection of down syndrome and other chromosomal anomalies in Israel

M. Shohat, A. Amiel, Z. Ben‐Neriah, 1995, Prenatal diagnosis.

Occurrence of four types of growth hormone-related dwarfism in Israeli communities

Z. Zadik, Z. Josefsberg, J. Chemke, 1981, European Journal of Pediatrics.

Autosomal recessive inheritance of Nager acrofacial dysostosis.

B. Mogilner, D. Ophir, J. Chemke, 1988, Journal of medical genetics.

A familial syndrome of central nervous system and ocular malformations

B. Czernobilsky, J. Chemke, Y. Barishak, 1975, Clinical genetics.

Prenatal diagnosis of cystic fibrosis: Ultrasonographic appearance of meconium ileus in the fetus

M. Lancet, B. Caspi, U. Elchalal, 1988 .

Genetic Counselling for Trisomy 20 Mosaicism in Amniotic Fluid Cell Cultures

J. Chemke, R. Nisani, S. Rappaport, 1984, Acta obstetricia et gynecologica Scandinavica.

Philadelphia chromosome in idiopathic acquired sideroblastic anemia.

A. Berrebi, R. Bruck, J. Chemke, 1984, Acta Haematologica.

Pure trisomy 17p in 60% of cells

F. Shabtai, I. Halbrecht, E. Elian, 2004, Human Genetics.

Prenatal diagnosis of SLO syndrome.

J. Chemke, Z. Gelman-Kohan, 1995, American journal of medical genetics.

Testicular feminisation syndrome: unusual gonadal histology in an elderly patient.

M. Lancet, B. Czernobilsky, A. Shani, 1977, Journal of medical genetics.