C. Legum

发表

Jadassohn-type anetoderma in association with keratoconus and cataract.

S. Brenner, P. Nemet, C. Legum, 1977, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.

Prenatal diagnosis of mucolipidosis IV by electron microscopy.

A. Ornoy, M. Cohen, G. Bach, 1977, The Journal of pediatrics.

Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype.

F. Muntoni, V. Dubowitz, Y. Nevo, 2003, The Israel Medical Association journal : IMAJ.

Familial colon cancer in the Tel‐Aviv area and the influence of ethnic origin

Z. Fireman, W. Kimberling, A. Figer, 1987, Cancer.

Family history of colorectal cancer as a marker of potential malignancy within a screening program

Z. Fireman, A. Figer, H. Lynch, 1987, Cancer.

Prenatal diagnosis of vitamin D-dependent rickets, type II: response to 1,25-dihydroxyvitamin D in amniotic fluid cells and fetal tissues.

Z. Hochberg, Y. Weisman, Z. Spirer, 1990, The Journal of clinical endocrinology and metabolism.

Novel mutations in the emerin gene in Israeli families

A. Orr-Urtreger, Y. Nevo, Y. Yaron, 2001, Human mutation.

High frequency of a common Bloom syndrome Ashkenazi mutation among Jews of Polish origin.

J. Groden, A. Orr-Urtreger, Y. Yaron, 1998, Genetic testing.

Mutations of the adenomatous polyposis coli and p53 genes in a child with Turcot's syndrome.

S. Avigad, I. Cohen, R. Zaizov, 1998, Cancer letters.

Y. Nevo, U. Kramer, D. Soffer, 1998, American journal of medical genetics.

A molecular survey of Israeli Duchenne and Becker muscular dystrophy patients.

Y. Shiloh, M. Glassner, C. Legum, 1994, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Prenatal diagnosis microscopy of mucolipidosis IV by electron

A. Ornoy, G. Bach, Y. Beyth, 1977 .

Studies on leukocyte bracher enzyme activity in a family with type IV glycogenosis.

C. Legum, H. Nitowsky, 1969, The Journal of pediatrics.

Familial adenomatous polyposis at the Tel Aviv Medical Center: demographic and clinical features

A. Orr-Urtreger, P. Rozen, C. Legum, 2004, Familial Cancer.

Further observations on familial hypobetaliproteinaemia

C. Legum, D. Lotan, I. Tamir, 1976, Clinical genetics.

Radiological aspects of the vertebral components of osteochondrodysplasias.

C. Legum, S. Schorr, 1977, The British journal of radiology.

Genetic Counseling:

C. Legum, H. Nitowsky, HAROLD M. NITOWSKY, 1971, Advances in Pediatrics.

The genetic mucopolysaccharidoses and mucolipidoses: review and comment.

E. Berman, C. Legum, S. Schorr, 1976, Advances in pediatrics.

SECOND‐TRIMESTER MATERNAL SERUM ALPHA‐FETOPROTEIN, HUMAN CHORIONIC GONADOTROPIN, AND UNCONJUGATED OESTRIOL AFTER EARLY TRANSVAGINAL MULTIFETAL PREGNANCY REDUCTION

Y. Yaron, J. Lessing, A. Amit, 1996, Prenatal diagnosis.

A New Variant of Mannosidosis with Increased Residual Enzymatic Activity and Mild Clinical Manifestation

A. Ornoy, G. Bach, C. Legum, 1978, Pediatric Research.

Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.

Y. Shiloh, C. Legum, R. Shomrat, 1994, American journal of medical genetics.

Spondyloenchondrodysplasia. Enchondromatomosis with severe platyspondyly in two brothers.

C. Legum, S. Schorr, M. Ochshorn, 1976, Radiology.

Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer.

P Rozen, A. Orr-Urtreger, P. Rozen, 1999, Gastroenterology.

Acute neonatal isovaleric acidemia. A report of two cases.

Z. Spirer, C. Legum, V. Zakut, 1975, Israel journal of medical sciences.

Detection of Duchenne muscular dystrophy gene products in amniotic fluid and chorionic villus sampling cells

M. Brusel, U. Nudel, D. Yaffe, 1993 .

Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.

J. Beckmann, J. Burgunder, J. Loiselet, 1997, American journal of human genetics.

Partial trisomy D: a diagnostic and cytogenetic dilemma.

M. Cohen, C. Legum, A. Rosenmann, 1976, Journal of medical genetics.

Heterogeneity and pleiotropism in the Moebius syndrome

P. Nemet, C. Legum, V. Godel, 1981, Clinical genetics.

The Dyggve-Melchio-Clausen syndrome.

M. Hirsch, C. Legum, S. Schorr, 1977, AJR. American journal of roentgenology.

Developmental dental anomalies in chondroectodermal dysplasia (Ellis-van Creveld syndrome).

C. Legum, E. Amir, H. Sarnat, 1980, ASDC journal of dentistry for children.

A New Phenotypic Variant of α-L-Iduronidase Deficiency1

M. Cohen, G. Bach, C. Legum, 1978 .

Cleidocranial dysplasia. A family study.

C. Legum, S. Schorr, I. Reider-Grosswasser, 1979, Clinical radiology.

Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy.

Y. Shiloh, C. Legum, R. Shomrat, 1992, American journal of medical genetics.

A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies

J. Beckmann, J. Burgunder, N. Bourg, 1999, Neuromuscular Disorders.

Notable intrafamilial phenotypic variability in a kindred with familial adenomatous polyposis and an APCmutation in exon 9

P. Rozen, C. Legum, R. Shomrat, 1999, Gut.

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

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

One SHOX Can Make You Short

M. Shohat, O. Nahum, C. Legum, 2002 .

Solar activity cycle and the incidence of foetal chromosome abnormalities detected at prenatal diagnosis

M. Shohat, M. Fejgin, G. Barkai, 1995, International journal of biometeorology.

Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations

D. Bercovich, A. Orr-Urtreger, Y. Yaron, 2002, Human mutation.

Doppler velocimetry of the umbilical artery as a predictor of outcome in pregnancies characterized by elevated beta-subunit human chorionic gonadotropin.

M. Evans, A. Jaffa, Y. Yaron, 1997, Fetal diagnosis and therapy.

Doppler velocimetry of the umbilical artery as a predictor of pregnancy outcome in pregnancies characterized by elevated maternal serum alpha-fetoprotein and normal amniotic fluid alpha-fetoprotein.

A. Jaffa, J. Lessing, Y. Yaron, 1997, Fetal diagnosis and therapy.

Prenatal diagnosis of Lesch‐Nyhan syndrome: Experience with three fetuses at risk

G. Barkai, C. Legum, B. Goldman, 1989, Prenatal Diagnosis.

Autosomal recessive colobomatous microphthalmia.

J. Zlotogora, D. Benezra, C. Legum, 1994, American journal of medical genetics.

Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family.

Y. Shiloh, H. Goebel, M. Frydman, 1995, American journal of medical genetics.

A Hitherto Undescribed Ocular Sign of Down's Syndrome in the Crying Newborn

C. Legum, Israel Heyman, 1975, Developmental medicine and child neurology.

Down Syndrome Prevention Program in a Population With an Older Maternal Age

M. Shohat, Z. Borochowitz, Y. Romem, 1995, Obstetrics and gynecology.

Partial trisomy D: a diagnostic and cytogenetic dilemma*

C. Legum, 2022 .

Ultrastructure of cultured fibroblasts in mucolipidosis type IV.

C. Legum, N. Livni, 1976, Experimental cell biology.

Fetal muscle biopsy as a diagnostic tool in Duchenne muscular dystrophy

A. Orr-Urtreger, Y. Nevo, S. Harel, 1999, Prenatal diagnosis.