A citation-based method for searching scientific literature


List of co-cited articles
269 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity




Cyclopia as a result of an unbalanced familial translocation, rcp(7;18)(q34;q21)
R D Smart, J Ross, G Amann, M M Nelson. Am J Med Genet 1986
18
88

A lethal presentation of de novo deletion 7q.
L E McMorrow, I R Toth, M M Gluckson, A Leff, S R Wolman. J Med Genet 1987
20
60

A girl with karyotype 46,XX,del(7)(pter leads to q32:).
U Friedrich, O Osterballe, S Stenbjerg, J Jørgensen. Hum Genet 1979
33
33



Duplication of part of chromosome 1q: clinical report and review of literature.
V V Michels, C L Berseth, J F O'Brien, G Dewald. Am J Med Genet 1984
26
34


Duplication 3p21----3pter and cyclopia.
D N Kurtzman, D L Van Dyke, C A Rich, L Weiss. Am J Med Genet 1987
25
36

Case of cyclopia with an unbalanced karyotype attributable to a balanced 3/7 translocation.
K F Bürrig, J Gebauer, R Terinde, P Pfitzer. Clin Genet 1989
16
56

Familial holoprosencephaly associated with a translocation breakpoint at chromosomal position 7q36.
A G Hatziioannou, C M Krauss, M B Lewis, T D Halazonetis. Am J Med Genet 1991
29
27

Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases.
R S Young, D D Weaver, M K Kukolich, N A Heerema, C G Palmer, E L Kawira, H A Bender. Am J Med Genet 1984
67
18

Partial trisomy 1q syndrome.
H Rehder, U Friedrich. Clin Genet 1979
33
21

Partial trisomy 1 (q42 leads to ter).
J Leisti, P Aula. Clin Genet 1980
26
26

Partial trisomy of the long arm of human chromosome 1 as demostrated by in situ hybridization with 5S ribosomal RNA.
D M Steffensen, E H Chu, D P Speert, P M Wall, K Meilinger, R P Kelch. Hum Genet 1977
63
16

"De novo" trisomy 1q32 leads to 1qter and monosomy 3p25 leads to 3pter.
E Yunis, H Egel, R Zúñiga, E Ramirez, O M Torres de Caballero, M Leibovici. Hum Genet 1977
34
20



Dup(3)(p2----pter) in two families, including one infant with cyclopia.
G Gimelli, C Cuoco, M Lituania, M Cordone, M Aricò, E Bianchi, P Maraschio, O Zuffardi. Am J Med Genet 1985
24
29


Chromosome 7 abnormalities in parents of children with holoprosencephaly and hydronephrosis.
I W Lurie, H G Ilyina, L V Podleschuk, L B Gorelik, D V Zaletajev. Am J Med Genet 1990
24
29

Holoprosencephaly in a fetus with a 46,XX,der(7), t(7;8)(q36.1;p12) mat karyotype.
A Kleczkowska, J P Fryns, P Moerman, K Vandenberghe, H Van den Berghe. Ann Genet 1990
13
53



Partial distal 1q trisomy. A distinct clinical dysmorphic syndrome in adulthood.
J P Fryns, A de Muelenaere, J Pedersen, H Van Den Berghe. Ann Genet 1980
21
28


Single central incisor in familial holoprosencephaly.
S A Berry, M E Pierpont, R J Gorlin. J Pediatr 1984
57
13

Holoprosencephaly in infants of diabetic mothers.
M Barr, J W Hanson, K Currey, S Sharp, H Toriello, R D Schmickel, G N Wilson. J Pediatr 1983
158
13

Triploidy with cyclopia and identical HLA alleles in the parents.
J C Lambert, P Philip, G Charpentier, M Ferrari, M Donzeau, N Ayraud. J Med Genet 1984
10
60

Ultrasonic findings with holoprosencephaly.
L M Hill, R Breckle, C R Bonebrake. J Reprod Med 1982
18
33

Congenital heart defect in a patient with deletion of chromosome 7q.
G E Tiller, M S Watson, L M Duncan, S B Dowton. Am J Med Genet 1988
14
42

Terminal deletions of the long arm of chromosome 7: five new cases.
M H Bogart, C Cunniff, C Bradshaw, K L Jones, O W Jones. Am J Med Genet 1990
24
25

Inheritance and phenotypic expression of a t(7;9)(q36;q34)mat.
C M Krauss, K J Liptak, A Aggarwal, D Robinson. Am J Med Genet 1989
13
46

Cyclopia and other anomalies following maternal ingestion of salicylates.
R Benawra, H H Mangurten, D R Duffell. J Pediatr 1980
47
13

Partial trisomy 1q due to tandem duplication.
S Flatz, C Fonatsch. Clin Genet 1979
40
12

Genetic heterogeneity of cebocephaly.
L B Holmes, S Driscoll, L Atkins. J Med Genet 1974
33
15

Trisomy 18 and cyclopia.
A F Lang, F M Schlager, H A Gardner. Teratology 1976
30
16

An infant with trisomy 6q21 leads to 6qter.
R L Neu, J U Gallien, N Steinberg-Warren, R J Wynn, R M Bannerman. Ann Genet 1981
14
35

Holoprosencephaly and trisomy 21 in a child born to a nondiabetic mother.
M Urioste, E Valcarcel, M A Gomez, I Pinel, R Garcia de León, A Diaz de Bustamante, R Tebar, M L Martinez-Frias. Am J Med Genet 1988
29
17


Cyclopism as a hereditary malformation.
P Pfitzer, H Müntefering. Nature 1968
29
17

Terminal long arm deletion of chromosome 7 and retino-choroidal coloboma.
K Taysi, R M Burde, J R Rohrbaugh. Ann Genet 1982
18
27

Caudal deficiency sequence in 7q terminal deletion.
C Schrander-Stumpel, J Schrander, J P Fryns, G Hamers. Am J Med Genet 1988
24
20

Single central maxillary incisor and holoprosencephaly.
H Hattori, T Okuno, T Momoi, K Kataoka, H Mikawa, K Shiota. Am J Med Genet 1987
37
13

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
E Belloni, M Muenke, E Roessler, G Traverso, J Siegel-Bartelt, A Frumkin, H F Mitchell, H Donis-Keller, C Helms, A V Hing,[...]. Nat Genet 1996
487
9

Triploidy in 40 human spontaneous abortuses: assessment of phenotype in embryos.
M J Harris, B J Poland, F J Dill. Obstet Gynecol 1981
20
20

Partial trisomy 3p in two siblings: clinical and pathological findings.
N Van Regemorter, E Vamos, Y Gillerot, V Viteux, F Hayez, A Pardou, J Flament-Durand. Eur J Pediatr 1983
21
19


Cyclopia associated with triploidy and hydatidiform mole: a case report.
L Deligdisch, C Legum, M R Peyser, R Toaff. Teratology 1978
16
25


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.