Preterm blood counts vary with sampling site.

Por Shohat, M
Publicado em 1987

Phenotypic expression of the first liveborn 68,XX triploid newborn.

Por Merlob, P, Naor, N, Shohat, M
Publicado em 1991

Effects of consanguineous marriage on reproductive outcome in an Arab community in Israel.

Por Jaber, L, Merlob, P, Gabriel, R, Shohat, M
Publicado em 1997

Familial hypothyroidism with autosomal dominant inheritance.

Por Mimouni, M, Mimouni-Bloch, A, Schachter, J, Shohat, M
Publicado em 1996

Transient tachypnoea of the newborn and asthma.

Por Shohat, M, Levy, G, Levy, I, Schonfeld, T, Merlob, P
Publicado em 1989

Hypertension in Israeli adolescents: prevalence according to weight, sex and parental origin.

Por Shohat, M, Shohat, T, Mimouni, M, Nitzan, M, Danon, Y L
Publicado em 1989

Childhood asthma and growth outcome.

Por Shohat, M, Shohat, T, Kedem, R, Mimouni, M, Danon, Y L
Publicado em 1987

Retinopathy of prematurity: incidence and treatment.

Por Reisner, S H, Amir, J, Shohat, M, Krikler, R, Nissenkorn, I, Ben-Sira, I
Publicado em 1985

A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.

Por Shohat, M, Lotan, R, Magal, N, Shohat, T, Fischel-Ghodsian, N, Rotter, J I, Jaber, L
Publicado em 1997

Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity

Por Basel-Vanagaite, L, Alkelai, A, Straussberg, R, Magal, N, Inbar, D, Mahajna, M, Shohat, M
Publicado em 2003

Sensorineural deafness inherited as a tissue specific mitochondrial disorder.

Por Jaber, L, Shohat, M, Bu, X, Fischel-Ghodsian, N, Yang, H Y, Wang, S J, Rotter, J I
Publicado em 1992

Overexpression of a set of genes, including WISP-1, common to pulmonary metastases of both mouse D122 Lewis lung carcinoma and B16-F10.9 melanoma cell lines

Por Margalit, O, Eisenbach, L, Amariglio, N, Kaminski, N, Harmelin, A, Pfeffer, R, Shohat, M, Rechavi, G, Berger, R
Publicado em 2003

PREGNANCY: Triple-Test Screening in In Vitro Fertilization Pregnancies

Por Bar-Hava, I., Yitzhak, M., Krissi, H., Shohat, M., Shalev, J., Czitron, B., Ben-Rafael, Z., Orvieto, R.
Publicado em 2001

Candidate locus for a nuclear modifier gene for maternally inherited deafness.

Por Bykhovskaya, Y, Estivill, X, Taylor, K, Hang, T, Hamon, M, Casano, R A, Yang, H, Rotter, J I, Shohat, M, Fischel-Ghodsian, N
Publicado em 2000

The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneity.

Por Shohat, M, Bu, X, Shohat, T, Fischel-Ghodsian, N, Magal, N, Nakamura, Y, Schwabe, A D, Schlezinger, M, Danon, Y, Rotter, J I
Publicado em 1992

Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families.

Por Levy-Lahad, E, Catane, R, Eisenberg, S, Kaufman, B, Hornreich, G, Lishinsky, E, Shohat, M, Weber, B L, Beller, U, Lahad, A, Halle, D
Publicado em 1997

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non‐syndromic mental retardation

Por Basel‐Vanagaite, L, Attia, R, Yahav, M, Ferland, R J, Anteki, L, Walsh, C A, Olender, T, Straussberg, R, Magal, N, Taub, E, Drasinover, V, Alkelai, A, Bercovich, D, Rechavi, G, Simon, A J, Shohat, M
Publicado em 2006

Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246.

Por Levy, E. N., Shen, Y., Kupelian, A., Kruglyak, L., Aksentijevich, I., Pras, E., Balow, J. E., Linzer, B., Chen, X., Shelton, D. A., Gumucio, D., Pras, M., Shohat, M., Rotter, J. I., Fischel-Ghodsian, N., Richards, R. I., Kastner, D. L.
Publicado em 1996

OR13-002 Recessive mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause systemic and cutaneous polyarteritis nodosa (PAN)

Por Levy-Lahad, E, Elkan-Navon, P, Segel, R, Pierce, SB, Walsh, T, Barash, J, Padeh, S, Zlotogorski, A, Berkun, YY, Press, JJ, Mukamel, M, Hashkes, PJ, Harel, LL, Tekin, M, Yalcinkaya, F, Kasapcopur, O, Emirogullari, EF, Lee, MK, Klevit, RE, Renbaum, PF, Weinberg-Shukron, A, Zeligson, S, Marek-Yagel, D, Shohat, M, Singer, A, Pras, E, Rubinow, AA, Anikster, Y, King, M-C
Publicado em 2013