| Ident. | Authors (with country if any) | Title |
|---|
| 001182 (2008) |
Tanya L. Gillan [Canada] ; Christine Davies [Canada] ; A. Micheil Innes [Canada] ; Jayda Howard [Canada] ; Lisa Graham [Canada] ; Judy Chernos [Canada] ; Peter J. Bridge [Canada] ; Jillian S. Parboosingh [Canada] | An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier |
| 002602 (2002) |
A. L. Buonadonna ; F. Cariola ; E. Caroppo [Italie] ; A. Di Carlo ; P. Fiorente ; M. C. Valenzano ; G. D'Amato [Italie] ; M. Gentile | Molecular and cytogenetic characterization of an azoospermic male with a de-novo Y;14 translocation and alternate centromere inactivation |
| 002C87 (2001) |
S. Prasad [Royaume-Uni] ; P. Puri [Royaume-Uni] ; K. Sisley [Royaume-Uni] ; S. Prasad [Royaume-Uni] ; P. Puri [Royaume-Uni] ; K. Sisley [Royaume-Uni] ; A. Parsons [Royaume-Uni] ; I G Rennie [Royaume-Uni] | Cytogenetic analysis in ocular lymphoma |
| 003D61 (1998) |
Michio Teraoka [Japon] ; Koji Narahara [Japon] ; Yuji Yokoyama [Japon] ; Kazushiro Tsuji [Japon] ; Kiyoshi Kikkawa [Japon] ; Satoko Ito [Japon] ; Kiyoko Koyama [Japon] ; Yoshiki Seino [Japon] | 45,X/46,X,idic(Yq) mosaicism: Clinical, cytogenetic, and molecular studies in four individuals |
| 004008 (1997) |
S. F. Witchel [États-Unis] ; S. L. Wenger [États-Unis] ; E. P. Hoffman [États-Unis] | Molecular and Cytogenetic Studies of X Inactivation in a Patient with 46, X, del(X)(q22) |
| 004508 (1996) |
Chih-Ping Chen [République populaire de Chine] ; Fen-Fen Liu [République populaire de Chine] ; Sheau-Wen Jan [République populaire de Chine] ; Chen-Chi Lee [République populaire de Chine] ; Dai-Dyi Town [République populaire de Chine] ; Chung-Chi Lan [République populaire de Chine] | Cytogenetic evaluation of cystic hygroma associated with hydrops fetalis, oligohydramnios or intrauterine fetal death: the roles of amniocentesis, postmortem chorionic villus sampling and cystic hygroma paracentesis |
| 004896 (1995) |
T. Kuznetzova [Russie] ; A. Baranov [Russie] ; N. Schwed [Russie] ; T. Ivaschenko [Russie] ; P. Malet [Russie] ; M. Giollant [Russie] ; G A Savitsky [Russie] ; V. Baranov [Russie] | Cytogenetic and molecular findings in patients with Turner's syndrome stigmata. |
| 004897 (1995) |
Vijay Tonk [États-Unis] ; Herman E. Wyandt [États-Unis] ; Peter Osella [États-Unis] ; James Skare [États-Unis] ; Bai Lin Wu [États-Unis] ; Bassem Haddad [États-Unis] ; Aubrey Milunsky [États-Unis] | Cytogenetic and molecular cytogenetic studies of a case of interstitial deletion of proximal 15q |
| 004898 (1995) |
C. G. Palmer [États-Unis, Suisse] ; J. Blouin [États-Unis, Suisse] ; M. J. Bull [États-Unis, Suisse] ; P. Breitfeld [États-Unis, Suisse] ; G. H. Vance [États-Unis, Suisse] ; T. Van Meter [États-Unis, Suisse] ; D. D. Weaver [États-Unis, Suisse] ; N. A. Heerema [États-Unis, Suisse] ; S. G. Colbern [États-Unis, Suisse] ; J. R. Korenberg [États-Unis, Suisse] ; S. E. Antonarakis [États-Unis, Suisse] ; X. Chen [États-Unis, Suisse] | Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia |
| 004B81 (1994) |
Louise Gil-Benso [Espagne] ; Concha L Pez-Ginés [Espagne] ; Pilar Soriano [Espagne] ; Sergio Almenar [Espagne] ; Carlos Vazquez [Espagne] ; Antonio Llombart-Bosch [Espagne] | Cytogenetic study of angiosarcoma of the breast |
| 004C28 (1994) |
A L Collins [Royaume-Uni] ; A E Cockwell [Royaume-Uni] ; P A Jacobs [Royaume-Uni] ; N R Dennis [Royaume-Uni] | A comparison of the clinical and cytogenetic findings in nine patients with a ring (X) cell line and 16 45,X patients. |
| 004E90 (1993) |
Roberto T. Zori [États-Unis] ; James R. Lupski [États-Unis] ; Zhang Heju [États-Unis] ; Frank Greenberg [États-Unis] ; James M. Killian [États-Unis] ; Brian A. Gray [États-Unis] ; Daniel J. Driscoll [États-Unis] ; Pragna I. Patel [États-Unis] ; Joleen L. Zackowski [États-Unis] | Clinical, cytogenetic, and molecular evidence for an infant with Smith–Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion |
| 005096 (1992) |
V. Petrovic [Australie] ; S. Nasioulas [Australie] ; C W Chow [Australie] ; L. Voullaire [Australie] ; M. Schmidt [Australie] ; H. Dahl [Australie] | Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies. |
| 005339 (1991) |
Lars Gunnar Kindblom [Suède] ; Göran Stenman [Suède] ; Lennart Angervall [Suède] | Morphological and cytogenetic studies of angiosarcoma in Stewart-Treves syndrome |
| 006400 (1982) |
J. R. Casley Coco [Argentine] ; Victor B. Penchaszadeh [Argentine] ; John M. Opitz | Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown cause |
| 006410 (1982) |
B. Goldman [Royaume-Uni] ; P. E. Polani [Royaume-Uni] ; M. G. Daker [Royaume-Uni] ; R. R. Aangel [Royaume-Uni] | Clinical and cytogenetic aspects of X‐chromosome deletions |
| 006507 (1981) |
F. G. Cassorla [États-Unis] ; B S. Emanuel [États-Unis] ; J. S. Parks [États-Unis] ; C. H. Wu [États-Unis] ; J. E. Wheeler [États-Unis] ; A. Tenore [États-Unis] | Cytogenetic and endocrine findings in a female with 45, X, t(Y;18) (p11;p11) |
| 006610 (1980) |
M. Ferraro ; A. De Capoa ; C. Mostacci ; F. Pelliccia ; P. Zulli ; M A Baldini ; Q. Di Nisio | Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations. |
| 006704 (1979) |
James White [États-Unis] ; Clare Crandall [États-Unis] ; Jeffrey S. Flier [États-Unis] ; Elizabeth S. Raveché [États-Unis] ; Joe-Hin Tjio [États-Unis] ; Robert L. Summitt | Cytogenetic studies of a male with sporadic intestinal lymphangiectasia: 45,X/46,XY mosaicism with pseudo‐ and hyperdiploid subpopulations in cultured tissues |
| 006C42 (1973) |
Hanna Kallio | Cytogenetic and Clinical Study on 100 Cases of Primary Amenorrhoea |
| 006D74 (1971) |
Margarete S. Mattevi [Brésil] ; Henry Wolff [Brésil] ; F. M. Salzano [Brésil] ; Maria C. Mallmann [Brésil] | Cytogenetic, clinical and genealogical analyses in a series of gonadal dysgenesis patients and their families |
