-
1
-
-
0003594832
-
Community control of genetic and congenital disorders
-
Alexandria, WHO Eastern Mediterranean Regional Office
-
Alwan A, Modell B: Community control of genetic and congenital disorders. EMRO Technical Publications Series 24. Alexandria, WHO Eastern Mediterranean Regional Office. 1997.
-
(1997)
EMRO Technical Publications Series 24
-
-
Alwan, A.1
Modell, B.2
-
3
-
-
0028343960
-
Autosomal recessive disorders among Arabs: An overview from Kuwait
-
Teebi AS: Autosomal recessive disorders among Arabs: An overview from Kuwait. J Med Genet 1994;31:224-233.
-
(1994)
J Med Genet
, vol.31
, pp. 224-233
-
-
Teebi, A.S.1
-
4
-
-
0030561976
-
Unique demographic situation in the United Arab Emirates
-
Al Hosani H, Czeizel AE: Unique demographic situation in the United Arab Emirates. Am J Med Genet 1996;61:1.
-
(1996)
Am J Med Genet
, vol.61
, pp. 1
-
-
Al Hosani, H.1
Czeizel, A.E.2
-
5
-
-
0034106974
-
A study of consanguinity in the Sultanate of Oman
-
Rajab A, Patton M: A study of consanguinity in the Sultanate of Oman. Ann Hum Biol 2000;3:321-326.
-
(2000)
Ann Hum Biol
, vol.3
, pp. 321-326
-
-
Rajab, A.1
Patton, M.2
-
7
-
-
0343744185
-
A five-year prospective study of the health of children in different ethnic groups, with particular reference to the effect of inbreeding
-
Bundey S, Alam H: A five-year prospective study of the health of children in different ethnic groups, with particular reference to the effect of inbreeding. Eur J Hum Genet 1992;24:1-15.
-
(1992)
Eur J Hum Genet
, vol.24
, pp. 1-15
-
-
Bundey, S.1
Alam, H.2
-
9
-
-
0042508737
-
Genetic heritage of the Old Order Mennonites of southeastern Pennsylvania
-
Puffenberger EG: Genetic heritage of the Old Order Mennonites of southeastern Pennsylvania. Am J Med Genet Part C 2003;121C:18-31.
-
(2003)
Am J Med Genet Part C
, vol.121 C
, pp. 18-31
-
-
Puffenberger, E.G.1
-
10
-
-
0036432819
-
The burden of genetic disorders in India and a framework for community control
-
Verma IC, Bijarnia S: The burden of genetic disorders in India and a framework for community control. Community Genet 2002;5:192-196.
-
(2002)
Community Genet
, vol.5
, pp. 192-196
-
-
Verma, I.C.1
Bijarnia, S.2
-
11
-
-
0034425405
-
Recessive Robinow syndrome, allelic to dominant brachydactily type B, is caused by mutation of ROR2
-
Afzal AR, Rajab A, Fenzke CD, Oldridge M, Blanko N, Ternes-Pereira E, Tuysuz B, Murday V, Patton MA, Wilkie A, Jeffery S: Recessive Robinow syndrome, allelic to dominant brachydactily type B, is caused by mutation of ROR2 (letter). Nat Genet 2000;25:419-422.
-
(2000)
Nat Genet
, vol.25
, pp. 419-422
-
-
Afzal, A.R.1
Rajab, A.2
Fenzke, C.D.3
Oldridge, M.4
Blanko, N.5
Ternes-Pereira, E.6
Tuysuz, B.7
Murday, V.8
Patton, M.A.9
Wilkie, A.10
Jeffery, S.11
-
12
-
-
19244377450
-
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22
-
Afzal AR, Rajab A, Fenske C, Crosby A, Lahiri N, Ternes-Pereira E, Murday VA, Houlston R, Patton MA, Jeffrey S: Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22. Hum Genet 2000;106:351-354.
-
(2000)
Hum Genet
, vol.106
, pp. 351-354
-
-
Afzal, A.R.1
Rajab, A.2
Fenske, C.3
Crosby, A.4
Lahiri, N.5
Ternes-Pereira, E.6
Murday, V.A.7
Houlston, R.8
Patton, M.A.9
Jeffrey, S.10
-
13
-
-
0033662239
-
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)
-
Nicole S, Davoine CS, Topaloglu H, Cattolico L, Barrai D, Beighton P, Ben Hamida C, Hammouda H, Cruaud C, White PS, Samson D, Urtizberea JA, Lehmann-Horn F, Weissenbach J, Hentati F, Fontaine B: Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia). Nat Genet 2000;26:480-483.
-
(2000)
Nat Genet
, vol.26
, pp. 480-483
-
-
Nicole, S.1
Davoine, C.S.2
Topaloglu, H.3
Cattolico, L.4
Barrai, D.5
Beighton, P.6
Ben Hamida, C.7
Hammouda, H.8
Cruaud, C.9
White, P.S.10
Samson, D.11
Urtizberea, J.A.12
Lehmann-Horn, F.13
Weissenbach, J.14
Hentati, F.15
Fontaine, B.16
-
14
-
-
2142751024
-
Spondyloepiphyseal dysplasia Omani type. A new recessive type of SED with progressive spinal involvement
-
Rajab A, Kunze J, Mundlos S: Spondyloepiphyseal dysplasia Omani type. A new recessive type of SED with progressive spinal involvement. Am J Med Genet 2004;126A:413-419.
-
(2004)
Am J Med Genet
, vol.126 A
, pp. 413-419
-
-
Rajab, A.1
Kunze, J.2
Mundlos, S.3
-
15
-
-
3042750623
-
Loss of chonroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement
-
Tiele H, Sakano M, Kitagawa K, Rajab A, Holme W, Ritter H, Leschik G, Nurnberg P, Mundlos S: Loss of chonroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement. Proc Natl Acad Sci USA 2004;101:10155-10160.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 10155-10160
-
-
Tiele, H.1
Sakano, M.2
Kitagawa, K.3
Rajab, A.4
Holme, W.5
Ritter, H.6
Leschik, G.7
Nurnberg, P.8
Mundlos, S.9
-
16
-
-
0032242375
-
Identification of cystic fibrosis mutations in the United Arab Emirates. Mutations in brief No 133. Online
-
Frossard PM, Girodon E, Dawson KP, Ghanem N, Plassa F, Lestringant GG, Gooseens M: Identification of cystic fibrosis mutations in the United Arab Emirates. Mutations in brief No 133. Online. Hum Mutat 1998;11:412-413.
-
(1998)
Hum Mutat
, vol.11
, pp. 412-413
-
-
Frossard, P.M.1
Girodon, E.2
Dawson, K.P.3
Ghanem, N.4
Plassa, F.5
Lestringant, G.G.6
Gooseens, M.7
-
17
-
-
0034570413
-
Study of hemoglobinopathies in Oman through a national register
-
Rajab AG, Patton MA, Modell B: Study of hemoglobinopathies in Oman through a national register. Saudi Med J 2000;21:1168-1172.
-
(2000)
Saudi Med J
, vol.21
, pp. 1168-1172
-
-
Rajab, A.G.1
Patton, M.A.2
Modell, B.3
-
18
-
-
0036644298
-
2002 Heterogeneity for congenital generalized lipodystrophy in seventeen patients from Oman
-
Rajab A, Heathcote K, Joshi S, Jeffery S, Patton M: 2002 Heterogeneity for congenital generalized lipodystrophy in seventeen patients from Oman. Am J Med Genet 2002;110:219-225.
-
(2002)
Am J Med Genet
, vol.110
, pp. 219-225
-
-
Rajab, A.1
Heathcote, K.2
Joshi, S.3
Jeffery, S.4
Patton, M.5
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