A citation-based method for searching scientific literature

L M Hill, R Breckle, C R Bonebrake. J Reprod Med 1982
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.
R A Filly, D H Chinn, P W Callen. Radiology 1984
67
44

Ultrasound criteria for in utero diagnosis of microcephaly.
A B Kurtz, R J Wapner, C S Rubin, C Cole-Beuglet, R D Ross, B B Goldberg. J Clin Ultrasound 1980
49
38


Antenatal ultrasound diagnosis of holoprosencephaly: a case report.
D E Blackwell, J A Spinnato, G Hirsch, H R Giles, J Sackler. Am J Obstet Gynecol 1982
32
38

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
159
38


What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
33

Holoprosencephaly in a Down syndrome child.
S Y Pi, R M Fineman, S D Wing, M Grunnet, G Chan. Am J Med Genet 1980
26
33


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
27

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
27


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
27




Descriptive neuropathology of chromosomal disorders in man.
F Gullotta, H Rehder, A Gropp. Hum Genet 1981
42
27



Review. In utero sonographic diagnosis of fetal cerebral anomalies.
H Hidalgo, J Bowie, E R Rosenberg, P C Ram, K Ford, E Lipsit. AJR Am J Roentgenol 1982
39
22

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
22

47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformations.
N D Dinno, G L Silvey, B Weisskopf. Clin Genet 1974
24
22


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
28

Single central incisor in familial holoprosencephaly.
S A Berry, M E Pierpont, R J Gorlin. J Pediatr 1984
57
22

Triploidy in 40 human spontaneous abortuses: assessment of phenotype in embryos.
M J Harris, B J Poland, F J Dill. Obstet Gynecol 1981
20
22

Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
Y E Hsia, M Bratu, A Herbordt. Pediatrics 1971
119
22

49,XXXXY syndrome.
P D Pallister. Am J Med Genet 1982
20
22



Prenatal detection of cyclopia associated with interstitial deletion of 2p.
H O Grundy, P Niemeyer, M K Rupani, V F Ward, E R Wassman. Am J Med Genet 1989
17
23

Holoprosencephaly and interstitial deletion of 2(p2101p2109).
W G Wilson, D E Shanks, K W Sudduth, K A Couper, J McIlhenny. Am J Med Genet 1989
15
26


Duplication 3p21----3pter and cyclopia.
D N Kurtzman, D L Van Dyke, C A Rich, L Weiss. Am J Med Genet 1987
25
22

The obstetric significance of holoprosencephaly.
F A Chervenak, G Isaacson, M J Mahoney, M Tortora, T Mesologites, J C Hobbins. Obstet Gynecol 1984
42
22


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
40

A male infant with holoprosencephaly, associated with ring chromosome 21.
D C Aronson, M C Jansweijer, J M Hoovers, P G Barth. Clin Genet 1987
24
22


A girl with karyotype 46,XX,del(7)(pter leads to q32:).
U Friedrich, O Osterballe, S Stenbjerg, J Jørgensen. Hum Genet 1979
33
22

Cyclopia and congenital cytomegalovirus infection.
P J Byrne, M M Silver, J M Gilbert, W Cadera, A K Tanswell. Am J Med Genet 1987
41
22



Diagnosis and management of fetal holoprosencephaly.
F A Chervenak, G Isaacson, J C Hobbins, U Chitkara, M Tortora, R L Berkowitz. Obstet Gynecol 1985
52
16

Familial agnathia-holoprosencephaly.
R M Pauli, J C Pettersen, S Arya, E F Gilbert. Am J Med Genet 1983
75
16

The spectrum of the DiGeorge syndrome.
M E Conley, J B Beckwith, J F Mancer, L Tenckhoff. J Pediatr 1979
326
16



A case of cyclopia. Role of environmental factors.
F Mollica, L Pavone, G Nuciforo, G Sorge. Clin Genet 1979
33
16

Prenatal diagnosis of a new syndrome: holoprosencephaly with hypokinesia.
R P Morse, E Rawnsley, S K Sargent, J M Graham. Prenat Diagn 1987
25
16


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.