A citation-based method for searching scientific literature

N D Dinno, G L Silvey, B Weisskopf. Clin Genet 1974
Times Cited: 24







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



Times Cited
  Times     Co-cited
Similarity


[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
M O Rethoré, L Larget-Piet, D Abonyi, M Boeswillwald, R Berger, S Carpentier, J Cruveiller, B Dutrillau, J Lafourcade, M Penneau,[...]. Ann Genet 1970
145
29

[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
M O Rethoré, H Hoehn, H D Rott, J Couturier, B Dutrillaux, J Lejeune. Humangenetik 1973
81
29


C 11-D 13-translocation in four generations.
H D Rott, G Schwanitz, K P Grosse, G Alexandrow. Humangenetik 1972
37
25

Partial 11q trisomy syndrome.
H Pihko, E Therman, I A Uchida. Hum Genet 1981
54
25

Trisomy 9q-. a variant of the 9p trisomy syndrome.
W R Centerwall, C A Mayeski, C C Cha. Humangenetik 1975
20
30

Partial trisomy 9 in the case of familial translocation 8/9 mat.
G Schwanitz, U Schamberger, H D Rott, V Wieczorek. Ann Genet 1974
29
25

A new case of trisomy for the short arm of No. 9 chromosome.
C Baccichetti, R Tenconi. J Med Genet 1973
36
25


[Partial trisomy 11q identified by study, with heat controlled denaturation, of the paternal balanced translocation].
J Tusques, J R Grislain, M J André, R Mainard, J M Rival, J L Cadudal, B Dutrillaux, J Lejeune. Ann Genet 1972
28
20


[On three cases of C trisomy].
J Lejeune, B Dutrillaux, M O Rethoré, R Berger, H Debray, P Veron, F Gorce, A Grossiord. Ann Genet 1969
41
20

Congenital malformations in autosomal trisomy syndromes.
J Warkany, E Passarge, L B Smith. Am J Dis Child 1966
221
20

Holoprosencephaly and agenesis of the corpus callosum: frequency of associated malformations.
K Jellinger, H Gross, E Kaltenbäck, W Grisold. Acta Neuropathol 1981
93
20




A case of trisomy 9p in a family with translocation 9/15.
P Balícek, J Zizka, J Lichý. Humangenetik 1975
22
22

Partial and complete trisomy 9: delineation of a trisomy 9 syndrome.
G R Sutherland, R F Carter, L L Morris. Hum Genet 1976
77
20


[Trisomy 9p : 2 further cases].
C Turleau, J de Grouchy, F Chavin-Colin, M Roubin, H Langmaid. Ann Genet 1974
32
20


A case with 46, XX, del (11) (q21).
J Faust, W Vogel, B Löning. Clin Genet 1974
44
16



Single central incisor in familial holoprosencephaly.
S A Berry, M E Pierpont, R J Gorlin. J Pediatr 1984
57
16

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
16

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

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
16


Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.
R A Filly, D H Chinn, P W Callen. Radiology 1984
66
16


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
16

Descriptive neuropathology of chromosomal disorders in man.
F Gullotta, H Rehder, A Gropp. Hum Genet 1981
42
16

Ultrasonic findings with holoprosencephaly.
L M Hill, R Breckle, C R Bonebrake. J Reprod Med 1982
18
22


[Chromosome 8 : complete trisomy and segmental trisomies].
M O Rethoré, A Aurias, J Couturier, B Dutrillaux, M Prieur, J Lejeune. Ann Genet 1977
61
16

[Partial trisomy 11q and familial translocation 11--22 (author's transl)].
F Giraud, J F Mattei, M G Mattei, R Bernard. Humangenetik 1975
26
16

[2 cases of trisomy 11q(q23.2-- qter) with the same abnormality of external genitalia].
C Laurent, M C Biemont, M Bethenod, L Cret, M David. Ann Genet 1975
33
16

[2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families].
A Aurias, C Turc, Y Michiels, P M Sinet, D Graveleau, J Lejeune. Ann Genet 1975
31
16


De novo trisomy 9pter leads to q13.
N B Kardon, H R Salwen, M A Krauss, J G Davis, E C Jenkins. Hum Genet 1977
6
66

The 9p- syndrome.
O S Alfi, G N Donnell, P W Allderdice, A Derencsenyi. Ann Genet 1976
57
16


Genetics of the +p9 syndrome.
I W Lurie, G I Lazjuk, D B Gurevich, S S Usoev. Hum Genet 1976
32
16

Trisomy for the distal half of the short arm of chromosome 9. A variant of the trisomy 9p syndrome.
R C Lewandowski, J J Yunis, R Lehrke, J O'Leary, K F Swaiman, O Sanchez. Am J Dis Child 1976
25
16

[Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father].
C Turleau, J De Grouchy, M Roubin, F Chavin-Colin, O Cachin. Ann Genet 1975
15
26

Trisomy 9p in a patient with a de novo 9/15 translocation.
P Jacobsen, N Hobolth, M Mikkelsen. Clin Genet 1975
22
18

Familial 'partial 9p' trisomy: six cases and four carriers in three generations.
W R Centerwall, K S Miller, L M Reeves. J Med Genet 1976
29
16

Trisomy 9p resulting from maternal 9/21 translocation.
I Sŭbrt, B Blehová, B Pallová. Hum Genet 1976
14
28


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.