-
1
-
-
62449256740
-
Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review
-
Akgül M, Ozkinay F, Ercal D, Cogulu O, et al. (2009). Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: report and review. J. Assist. Reprod. Genet. 26: 119-122.
-
(2009)
J. Assist. Reprod. Genet
, vol.26
, pp. 119-122
-
-
Akgül, M.1
Ozkinay, F.2
Ercal, D.3
Cogulu, O.4
-
2
-
-
0032586819
-
A survey of 1,000 cases referred for cytogenetic study to King Khalid University Hospital, Saudi Arabia
-
Al Husain M and Zaki OK (1999). A survey of 1,000 cases referred for cytogenetic study to King Khalid University Hospital, Saudi Arabia. Hum. Hered. 49: 208-214.
-
(1999)
Hum. Hered
, vol.49
, pp. 208-214
-
-
Al Husain, M.1
Zaki, O.K.2
-
4
-
-
38949145657
-
Culture and acculturation influences on Palestinian perceptions of prenatal genetic counseling
-
Awwad R, Veach PM, Bartels DM and LeRoy BS (2008). Culture and acculturation influences on Palestinian perceptions of prenatal genetic counseling. J. Genet. Couns. 17: 101-116.
-
(2008)
J. Genet. Couns
, vol.17
, pp. 101-116
-
-
Awwad, R.1
Veach, P.M.2
Bartels, D.M.3
Leroy, B.S.4
-
5
-
-
57349191531
-
Cytogenetic and Y chromosome microdeletion screening studies in infertile males with oligozoospermia and azoospermia in Southeast Turkey
-
Balkan M, Tekes S and Gedik A (2008). Cytogenetic and Y chromosome microdeletion screening studies in infertile males with oligozoospermia and azoospermia in Southeast Turkey. J. Assist. Reprod. Genet. 25: 559-565.
-
(2008)
J. Assist. Reprod. Genet
, vol.25
, pp. 559-565
-
-
Balkan, M.1
Tekes, S.2
Gedik, A.3
-
6
-
-
0028934438
-
Blood specimens from patients referred for cytogenetic analysis: Vanderbilt University experience from 1985 to 1992
-
Butler MG and Hamill T (1995). Blood specimens from patients referred for cytogenetic analysis: Vanderbilt University experience from 1985 to 1992. South Med. J. 88: 309-314.
-
(1995)
South Med. J
, vol.88
, pp. 309-314
-
-
Butler, M.G.1
Hamill, T.2
-
7
-
-
0005064379
-
Infertility and Recurrent Abortions
-
(Emery A and Rimoin D, eds.). Chapter 21. Churchill Livingstone, New York
-
Chandley AC (1990). Infertility and Recurrent Abortions. In: Principles and Practice of Medical Genetics (Emery A and Rimoin D, eds.). Chapter 21. Churchill Livingstone, New York, 313-319.
-
(1990)
Principles and Practice of Medical Genetics
, pp. 313-319
-
-
Chandley, A.C.1
-
8
-
-
4844230280
-
Cytogenetics of genetic counseling patients in Pelotas, Rio Grande do Sul, Brazil
-
Duarte AC, Cunha E, Roth JM, Ferreira FL, et al. (2004). Cytogenetics of genetic counseling patients in Pelotas, Rio Grande do Sul, Brazil. Genet. Mol. Res. 3: 303-308.
-
(2004)
Genet. Mol. Res
, vol.3
, pp. 303-308
-
-
Duarte, A.C.1
Cunha, E.2
Roth, J.M.3
Ferreira, F.L.4
-
10
-
-
0026145819
-
Trisomy 18 or Edwards' syndrome. A report of 4 clinical cases
-
Giaccardi A, Sardi R, Priora U, Vivalda M, et al. (1991). Trisomy 18 or Edwards' syndrome. A report of 4 clinical cases. Minerva Pediatr. 43: 343-349.
-
(1991)
Minerva Pediatr
, vol.43
, pp. 343-349
-
-
Giaccardi, A.1
Sardi, R.2
Priora, U.3
Vivalda, M.4
-
11
-
-
31844453953
-
Incidence of chromosome abnormalities in the Sultanate of Oman
-
Goud MT, Al-Harassi SM, Al-Khalili SA, Al-Salmani KK, et al. (2005). Incidence of chromosome abnormalities in the Sultanate of Oman. Saudi Med. J. 26: 1951-1957.
-
(2005)
Saudi Med. J
, vol.26
, pp. 1951-1957
-
-
Goud, M.T.1
Al-Harassi, S.M.2
Al-Khalili, S.A.3
Al-Salmani, K.K.4
-
12
-
-
0016588841
-
A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities
-
Hamerton JL, Canning N, Ray M and Smith S (1975). A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities. Clin. Genet. 8: 223-243.
-
(1975)
Clin. Genet
, vol.8
, pp. 223-243
-
-
Hamerton, J.L.1
Canning, N.2
Ray, M.3
Smith, S.4
-
13
-
-
0002418993
-
The Frequency of Chromosome Abnormalities Detected in Consecutive Newborn Studies - Differences Between Studies - Results by Sex and by Severity of Phenotypic Involvement
-
(Hook EB and Porter IH, eds.). Academic Press, New York
-
Hook EB and Hamerton JL (1977). The Frequency of Chromosome Abnormalities Detected in Consecutive Newborn Studies - Differences Between Studies - Results by Sex and by Severity of Phenotypic Involvement. In: Population Cytogenetics. Studies in Humans (Hook EB and Porter IH, eds.). Academic Press, New York, 63-79.
-
(1977)
Population Cytogenetics. Studies In Humans
, pp. 63-79
-
-
Hook, E.B.1
Hamerton, J.L.2
-
14
-
-
0003676646
-
An International System for Human Cytogenetic Nomenclature
-
International Software Consulting Network (ISCN), (Mitelman F, ed.). S. Karger Publishers Inc., Basel
-
International Software Consulting Network (ISCN) (1995). An International System for Human Cytogenetic Nomenclature. Recommendations of the International Standing Committee on Human Cytogenetic Nomenclature (Mitelman F, ed.). S. Karger Publishers Inc., Basel.
-
(1995)
Recommendations of The International Standing Committee On Human Cytogenetic Nomenclature
-
-
-
15
-
-
0033174755
-
Chromosome abnormalities in a referred population for suspected chromosomal aberrations: A report of 4117 cases
-
Kim SS, Jung SC, Kim HJ, Moon HR, et al. (1999). Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases. J. Korean Med. Sci. 14: 373-376.
-
(1999)
J. Korean Med. Sci
, vol.14
, pp. 373-376
-
-
Kim, S.S.1
Jung, S.C.2
Kim, H.J.3
Moon, H.R.4
-
16
-
-
0019428906
-
Incidence of major chromosomal abnormalities
-
Méhes K and Bajnoczky K (1981). Incidence of major chromosomal abnormalities. Clin. Genet. 19: 75-76.
-
(1981)
Clin. Genet
, vol.19
, pp. 75-76
-
-
Méhes, K.1
Bajnoczky, K.2
-
17
-
-
0021742023
-
Cytogenetic study on 282 patients with suspected chromosomal aberration
-
Milia A, Cardia S, Aste A, Santucci S, et al. (1984). Cytogenetic study on 282 patients with suspected chromosomal aberration. Eur. J. Obstet. Gynecol. Reprod. Biol. 18: 207-210.
-
(1984)
Eur. J. Obstet. Gynecol. Reprod. Biol
, vol.18
, pp. 207-210
-
-
Milia, A.1
Cardia, S.2
Aste, A.3
Santucci, S.4
-
18
-
-
0017420786
-
Incidence of major chromosome abnormalities in children
-
Patil SR, Lubs HA, Brown J, Cohen M, et al. (1977). Incidence of major chromosome abnormalities in children. Cytogenet. Cell Genet. 18: 3102-3106.
-
(1977)
Cytogenet. Cell Genet
, vol.18
, pp. 3102-3106
-
-
Patil, S.R.1
Lubs, H.A.2
Brown, J.3
Cohen, M.4
-
19
-
-
0016156825
-
C bands in human metaphase chromosomes treated by barium hydroxide
-
Salamanca F and Armendares S (1974). C bands in human metaphase chromosomes treated by barium hydroxide. Ann. Genet. 17: 135-136.
-
(1974)
Ann. Genet
, vol.17
, pp. 135-136
-
-
Salamanca, F.1
Armendares, S.2
-
20
-
-
0029853176
-
Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9
-
Samonte RV, Conte RA, Ramesh KH and Verma RS (1996). Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9. Hum. Genet. 98: 576-580.
-
(1996)
Hum. Genet
, vol.98
, pp. 576-580
-
-
Samonte, R.V.1
Conte, R.A.2
Ramesh, K.H.3
Verma, R.S.4
-
21
-
-
0034431543
-
Chromosomal investigations in patients with mental retardation and/or congenital malformations
-
Santos CB, Boy RT, Santos JM, Silva MPS, et al. (2000). Chromosomal investigations in patients with mental retardation and/or congenital malformations. Genet. Mol. Biol. 23: 703-707.
-
(2000)
Genet. Mol. Biol
, vol.23
, pp. 703-707
-
-
Santos, C.B.1
Boy, R.T.2
Santos, J.M.3
Silva, M.P.S.4
-
22
-
-
0015246254
-
A rapid banding technique for human chromosomes
-
Seabright M (1971). A rapid banding technique for human chromosomes. Lancet 2: 971-972.
-
(1971)
Lancet
, vol.2
, pp. 971-972
-
-
Seabright, M.1
-
23
-
-
69949132778
-
Cytogenetic Analyses in Medical Genetic Laboratory of Medical Biology Department in Afyonkarahisar Kocatepe University. Osmangazi
-
Solak M, Fistik T, Eser B, Söylemez Z, et al. (2007). Cytogenetic Analyses in Medical Genetic Laboratory of Medical Biology Department in Afyonkarahisar Kocatepe University. Osmangazi J. Med. 29: 93-99.
-
(2007)
J. Med
, vol.29
, pp. 93-99
-
-
Solak, M.1
Fistik, T.2
Eser, B.3
Söylemez, Z.4
-
24
-
-
0015423706
-
A simple technique for demonstrating centromeric heterochromatin
-
Sumner AT (1972). A simple technique for demonstrating centromeric heterochromatin. Exp. Cell Res. 75: 304-306.
-
(1972)
Exp. Cell Res
, vol.75
, pp. 304-306
-
-
Sumner, A.T.1
-
25
-
-
0014329459
-
Autosomal trisomy syndromes: A detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome
-
Taylor AI (1968). Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome. J. Med. Genet. 5: 227-252.
-
(1968)
J. Med. Genet
, vol.5
, pp. 227-252
-
-
Taylor, A.I.1
-
26
-
-
34447316749
-
Cytogenetic study of recurrent miscarriages and their parents
-
Tunç E, Demirhan O, Demir C and Tastemir D (2007). Cytogenetic study of recurrent miscarriages and their parents. Genetika 43: 545-552.
-
(2007)
Genetika
, vol.43
, pp. 545-552
-
-
Tunç, E.1
Demirhan, O.2
Demir, C.3
Tastemir, D.4
-
27
-
-
0018838859
-
Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: A report of 357 cases
-
Verma RS and Dosik H (1980). Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: a report of 357 cases. Clin. Genet. 17: 305-308.
-
(1980)
Clin. Genet
, vol.17
, pp. 305-308
-
-
Verma, R.S.1
Dosik, H.2
-
28
-
-
34249781710
-
Cytogenetic results of recurrent spontaneous abortions in Turkey
-
CR286-CR289
-
Yuce H, Tekedereli I and Elyas H (2007). Cytogenetic results of recurrent spontaneous abortions in Turkey. Med. Sci. Monit. 13: CR286-CR289.
-
(2007)
Med. Sci. Monit
, vol.13
-
-
Yuce, H.1
Tekedereli, I.2
Elyas, H.3
|