-
1
-
-
0023675203
-
The Cyprus thalassemia control
-
ANGASTINIOTIS, M., KYRIAKIDOU, S., and HADJIMINAS, M. (1988). The Cyprus thalassemia control. Birth defects, Original Articles Series 23, 417-432.
-
(1988)
Birth Defects, Original Articles Series
, vol.23
, pp. 417-432
-
-
Angastiniotis, M.1
Kyriakidou, S.2
Hadjiminas, M.3
-
2
-
-
0027268414
-
Screening for carriers of Tay Sachs disease in the Ultraorthodox Jewish community in Israel
-
BROIDE, ZEIGLER, M., ECKSTEIN, J., and BACH, G. (1993). Screening for carriers of Tay Sachs disease in the Ultraorthodox Jewish community in Israel. Am. J. Med. Genet. 47, 213-215.
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 213-215
-
-
Broide1
Zeigler, M.2
Eckstein, J.3
Bach, G.4
-
3
-
-
0030696315
-
Two connexin 26 mutations in an inbred kindred segregating non-syndromic deafness
-
CARRASQUILLO, M.M., ZLOTOGORA, J., BARGES, S., and CHAKRAVARTI, A. (1997). Two connexin 26 mutations in an inbred kindred segregating non-syndromic deafness. Hum. Mol. Gener. 6, 2163-2172.
-
(1997)
Hum. Mol. Gener.
, vol.6
, pp. 2163-2172
-
-
Carrasquillo, M.M.1
Zlotogora, J.2
Barges, S.3
Chakravarti, A.4
-
4
-
-
0028295887
-
Consanguineous mating in an Israeli-Arab community
-
JABER, L., BAILEY-WILSON, J.E., HAJ-YEHIA, M., HERMANDEZ, J., and SHOHAT, M. (1994). Consanguineous mating in an Israeli-Arab community. Arch. Pediatr. Adolesc. Med. 148, 412-415.
-
(1994)
Arch. Pediatr. Adolesc. Med.
, vol.148
, pp. 412-415
-
-
Jaber, L.1
Bailey-Wilson, J.E.2
Haj-Yehia, M.3
Hermandez, J.4
Shohat, M.5
-
5
-
-
0029798775
-
Twenty year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia carriers in high schools
-
MITCHELL, J.J., CAPUA, A., CLOW, C., and SCRIVER, C.R. (1996). Twenty year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia carriers in high schools. Am. J. Hum. Genet. 59, 793-798.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 793-798
-
-
Mitchell, J.J.1
Capua, A.2
Clow, C.3
Scriver, C.R.4
-
6
-
-
12444295768
-
-
Jerusalem, Israel
-
STATISTICAL ABSTRACTS OF ISRAEL. (2001). Central Bureau of statistics. Jerusalem, Israel.
-
(2001)
Central Bureau of Statistics
-
-
-
7
-
-
0003612858
-
Genetic Disorders among Arab Populations
-
No. 30. Oxford University Press, New York, Oxford
-
TEEBI, A.S., and FARAG, T.I. (1997). Genetic Disorders among Arab Populations, Oxford Monographs on Medical Genetics, No. 30. Oxford University Press, New York, Oxford.
-
(1997)
Oxford Monographs on Medical Genetics
-
-
Teebi, A.S.1
Farag, T.I.2
-
9
-
-
9844245885
-
Connexin 26 mutations associated with the most common form of nonsyndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
-
ZELANTE, L., GASPARINI, P., ESTEVILL, X., MELCHIONDA, S., D'AGRUMA, L., GOVEA, N., MILA, M., DELLA MONICA, M., JABER, L., SHOHAT, M., MANSFIELD, E., DELGROSSO, K., RAPPAPORT, E., SURREY, S., and FORTINA, P. (1997). Connexin 26 mutations associated with the most common form of nonsyndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Hum. Mol. Genet. 9, 1605-1609.
-
(1997)
Hum. Mol. Genet.
, vol.9
, pp. 1605-1609
-
-
Zelante, L.1
Gasparini, P.2
Estevill, X.3
Melchionda, S.4
D'Agruma, L.5
Govea, N.6
Mila, M.7
Della Monica, M.8
Jaber, L.9
Shohat, M.10
Mansfield, E.11
Delgrosso, K.12
Rappaport, E.13
Surrey, S.14
Fortina, P.15
-
10
-
-
0343183239
-
Genetic disorders among Palestinian Arabs 3: Autosomal recessive disorders in a single village
-
ZLOTOGORA, J., SHALEV, S., HABIBALLAH, H., and BARGES, S. (2000). Genetic disorders among Palestinian Arabs 3: autosomal recessive disorders in a single village. Am. J. Med. Genet. 92, 243-345.
-
(2000)
Am. J. Med. Genet.
, vol.92
, pp. 243-345
-
-
Zlotogora, J.1
Shalev, S.2
Habiballah, H.3
Barges, S.4
|