R van Zalen-Sprock, J M van Vugt, H J van der Harten, A W Nieuwint, H P van Geijn. J Ultrasound Med 1995
Times Cited: 16
Times Cited: 16
Times Cited
Times Co-cited
Similarity
First-trimester ultrasound diagnosis of holoprosencephaly: three case reports.
H S Wong, Y H Lam, M H Tang, L W Cheung, L K Ng, K W Yan. Ultrasound Obstet Gynecol 1999
H S Wong, Y H Lam, M H Tang, L W Cheung, L K Ng, K W Yan. Ultrasound Obstet Gynecol 1999
56
Prenatal diagnosis of alobar holoprosencephaly at 10 weeks of gestation.
C D Turner, S Silva, P Jeanty. Ultrasound Obstet Gynecol 1999
C D Turner, S Silva, P Jeanty. Ultrasound Obstet Gynecol 1999
50
First trimester diagnosis of holoprosencephaly with a Dandy-Walker malformation by transvaginal ultrasonography.
U Gembruch, A A Baschat, E Reusche, S J Wallner, M Greiwe. J Ultrasound Med 1995
U Gembruch, A A Baschat, E Reusche, S J Wallner, M Greiwe. J Ultrasound Med 1995
63
Early transvaginal sonographic diagnosis of alobar holoprosencephaly.
M Bronshtein, Z Wiener. Prenat Diagn 1991
M Bronshtein, Z Wiener. Prenat Diagn 1991
43
Alobar holoprosencephaly at 9 weeks gestational age visualized by two- and three-dimensional ultrasound.
H G Blaas, S H Eik-Nes, T Vainio, C V Isaksen. Ultrasound Obstet Gynecol 2000
H G Blaas, S H Eik-Nes, T Vainio, C V Isaksen. Ultrasound Obstet Gynecol 2000
37
First trimester sonographic diagnosis of holoprosencephaly.
T Tongsong, C Wanapirak, P Chanprapaph, S Siriangkul. Int J Gynaecol Obstet 1999
T Tongsong, C Wanapirak, P Chanprapaph, S Siriangkul. Int J Gynaecol Obstet 1999
50
First-trimester sonographic diagnosis of holoprosencephaly: value of the "butterfly" sign.
Waldo Sepulveda, Victor Dezerega, Cecilia Be. J Ultrasound Med 2004
Waldo Sepulveda, Victor Dezerega, Cecilia Be. J Ultrasound Med 2004
37
Holoprosencephaly in human embryos: epidemiologic studies of 150 cases.
E Matsunaga, K Shiota. Teratology 1977
E Matsunaga, K Shiota. Teratology 1977
31
Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases.
H G K Blaas, A G Eriksson, K A Salvesen, C V Isaksen, B Christensen, G Møllerløkken, S H Eik-Nes. Ultrasound Obstet Gynecol 2002
H G K Blaas, A G Eriksson, K A Salvesen, C V Isaksen, B Christensen, G Møllerløkken, S H Eik-Nes. Ultrasound Obstet Gynecol 2002
31
Diagnosis and management of fetal holoprosencephaly.
F A Chervenak, G Isaacson, J C Hobbins, U Chitkara, M Tortora, R L Berkowitz. Obstet Gynecol 1985
F A Chervenak, G Isaacson, J C Hobbins, U Chitkara, M Tortora, R L Berkowitz. Obstet Gynecol 1985
25
Holoprosencephaly in the west of Scotland 1975-1994.
M L Whiteford, J L Tolmie. J Med Genet 1996
M L Whiteford, J L Tolmie. J Med Genet 1996
25
[Prenatal diagnosis of holoprosencephaly. A series of twelve cases].
O Parant, M F Sarramon, M B Delisle, A Fournié. J Gynecol Obstet Biol Reprod (Paris) 1997
O Parant, M F Sarramon, M B Delisle, A Fournié. J Gynecol Obstet Biol Reprod (Paris) 1997
44
Alobar holoprosencephalic embryo detected via transvaginal sonography.
F González-Gómez, A Salamanca, M C Padilla, M Camara, R M Sabatel. Eur J Obstet Gynecol Reprod Biol 1992
F González-Gómez, A Salamanca, M C Padilla, M Camara, R M Sabatel. Eur J Obstet Gynecol Reprod Biol 1992
44
Holoprosencephaly: prenatal sonographic diagnosis.
D A Nyberg, L A Mack, A Bronstein, J Hirsch, R A Pagon. AJR Am J Roentgenol 1987
D A Nyberg, L A Mack, A Bronstein, J Hirsch, R A Pagon. AJR Am J Roentgenol 1987
25
In-vivo three-dimensional ultrasound reconstructions of embryos and early fetuses.
H G Blaas, S H Eik-Nes, S Berg, H Torp. Lancet 1998
H G Blaas, S H Eik-Nes, S Berg, H Torp. Lancet 1998
25
Fetal holoprosencephaly: associated malformations and chromosomal defects.
S M Berry, C Gosden, R J Snijders, K H Nicolaides. Fetal Diagn Ther 1990
S M Berry, C Gosden, R J Snijders, K H Nicolaides. Fetal Diagn Ther 1990
25
Three-dimensional sonographic evaluations of embryonic brain development.
Mi Suk Kim, Philippe Jeanty, Cheryl Turner, Bernard Benoit. J Ultrasound Med 2008
Mi Suk Kim, Philippe Jeanty, Cheryl Turner, Bernard Benoit. J Ultrasound Med 2008
25
Fundal uterine leiomyoma obscuring first-trimester transabdominal sonographic diagnosis of fetal holoprosencephaly. A case report.
E P Sakala, K L Gaio. J Reprod Med 1993
E P Sakala, K L Gaio. J Reprod Med 1993
60
De novo 7q36 deletion: breakpoint analysis and types of holoprosencephaly.
S G Frints, E F Schoenmakers, E Smeets, P Petit, J P Fryns. Am J Med Genet 1998
S G Frints, E F Schoenmakers, E Smeets, P Petit, J P Fryns. Am J Med Genet 1998
18
Duplication 3p21----3pter and cyclopia.
D N Kurtzman, D L Van Dyke, C A Rich, L Weiss. Am J Med Genet 1987
D N Kurtzman, D L Van Dyke, C A Rich, L Weiss. Am J Med Genet 1987
18
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly.
E Roessler, D E Ward, K Gaudenz, E Belloni, S W Scherer, D Donnai, J Siegel-Bartelt, L C Tsui, M Muenke. Hum Genet 1997
E Roessler, D E Ward, K Gaudenz, E Belloni, S W Scherer, D Donnai, J Siegel-Bartelt, L C Tsui, M Muenke. Hum Genet 1997
18
Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q.
G H Vance, C Nickerson, L Sarnat, A Zhang, O Henegariu, N Morichon-Delvallez, M G Butler, C G Palmer. Am J Med Genet 1998
G H Vance, C Nickerson, L Sarnat, A Zhang, O Henegariu, N Morichon-Delvallez, M G Butler, C G Palmer. Am J Med Genet 1998
30
Pallister-Hall syndrome associated with an unbalanced chromosome translocation.
J A Kuller, V A Cox, S A Schonberg, M Golabi. Am J Med Genet 1992
J A Kuller, V A Cox, S A Schonberg, M Golabi. Am J Med Genet 1992
18
Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly.
C P Chen, F F Liu, S W Jan, C L Lin, C C Lan. Clin Genet 1996
C P Chen, F F Liu, S W Jan, C L Lin, C C Lan. Clin Genet 1996
21
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
K F Bürrig, J Gebauer, R Terinde, P Pfitzer. Clin Genet 1989
18
Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology.
M M Cohen. Teratology 1989
M M Cohen. Teratology 1989
18
Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.
R A Filly, D H Chinn, P W Callen. Radiology 1984
R A Filly, D H Chinn, P W Callen. Radiology 1984
18
Early prenatal diagnosis of cyclopia associated with holoprosencephaly.
Z Tóth, K Csécsei, G Szeifert, O Török, Z Papp. J Clin Ultrasound 1986
Z Tóth, K Csécsei, G Szeifert, O Török, Z Papp. J Clin Ultrasound 1986
27
Early development of the forebrain and midbrain: a longitudinal ultrasound study from 7 to 12 weeks of gestation.
H G Blaas, S H Eik-Nes, T Kiserud, L R Hellevik. Ultrasound Obstet Gynecol 1994
H G Blaas, S H Eik-Nes, T Kiserud, L R Hellevik. Ultrasound Obstet Gynecol 1994
18
Intraventricular fused fornices: a specific sign of fetal lobar holoprosencephaly.
G Pilu, P Ambrosetto, F Sandri, G Tani, A Perolo, G Grisolia, G Ancora. Ultrasound Obstet Gynecol 1994
G Pilu, P Ambrosetto, F Sandri, G Tani, A Perolo, G Grisolia, G Ancora. Ultrasound Obstet Gynecol 1994
30
Diagnosis of fetal abnormalities at the 10-14-week scan.
A P Souka, K H Nicolaides. Ultrasound Obstet Gynecol 1997
A P Souka, K H Nicolaides. Ultrasound Obstet Gynecol 1997
18
Screening for fetal anomalies in the 12th week of pregnancy by transvaginal sonography in an unselected population.
L Hernádi, M Töröcsik. Prenat Diagn 1997
L Hernádi, M Töröcsik. Prenat Diagn 1997
18
Screening for fetal anomalies by ultrasound at 14 and 21 weeks.
G D'Ottavio, Y J Meir, M A Rustico, V Pecile, L Fischer-Tamaro, G Conoscenti, R Natale, G P Mandruzzato. Ultrasound Obstet Gynecol 1997
G D'Ottavio, Y J Meir, M A Rustico, V Pecile, L Fischer-Tamaro, G Conoscenti, R Natale, G P Mandruzzato. Ultrasound Obstet Gynecol 1997
18
Detection of fetal structural abnormalities at the 11-14 week ultrasound scan.
M H B Carvalho, M L Brizot, L M Lopes, C H Chiba, S Miyadahira, M Zugaib. Prenat Diagn 2002
M H B Carvalho, M L Brizot, L M Lopes, C H Chiba, S Miyadahira, M Zugaib. Prenat Diagn 2002
18
Fetal omphalocele detected early in pregnancy: associated anomalies and outcomes.
Shraga Blazer, Etan Z Zimmer, Ayala Gover, Moshe Bronshtein. Radiology 2004
Shraga Blazer, Etan Z Zimmer, Ayala Gover, Moshe Bronshtein. Radiology 2004
18
Ultrasonographically detectable markers of fetal chromosomal abnormalities.
K H Nicolaides, R J Snijders, C M Gosden, C Berry, S Campbell. Lancet 1992
K H Nicolaides, R J Snijders, C M Gosden, C Berry, S Campbell. Lancet 1992
12
Reliable criteria for the prenatal sonographic diagnosis of alobar holoprosencephaly.
M F Greene, B R Benacerraf, F D Frigoletto. Am J Obstet Gynecol 1987
M F Greene, B R Benacerraf, F D Frigoletto. Am J Obstet Gynecol 1987
12
What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
12
Autosomal imbalance syndromes: genetic interactions and the origin of congenital malformations in aneuploidy syndromes.
I W Lurie. Am J Med Genet 1993
I W Lurie. Am J Med Genet 1993
12
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
N Van Regemorter, E Vamos, Y Gillerot, V Viteux, F Hayez, A Pardou, J Flament-Durand. Eur J Pediatr 1983
12
The dup(3)(p25 leads to pter) syndrome: a case with holoprosencephaly.
N J Martin, B G Steinberg. Am J Med Genet 1983
N J Martin, B G Steinberg. Am J Med Genet 1983
12
Prenatal diagnosis of a dup(3p) with holoprosencephaly.
Y Gillerot, J Hustin, L Koulischer, V Viteux. Am J Med Genet 1987
Y Gillerot, J Hustin, L Koulischer, V Viteux. Am J Med Genet 1987
12
[Familial occurrence of cyclops over several generations].
P Pfitzer, M Splitt, H Müntefering, J E Friesenecker. Verh Dtsch Ges Pathol 1982
P Pfitzer, M Splitt, H Müntefering, J E Friesenecker. Verh Dtsch Ges Pathol 1982
33
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
G Gimelli, C Cuoco, M Lituania, M Cordone, M Aricò, E Bianchi, P Maraschio, O Zuffardi. Am J Med Genet 1985
12
Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1.
N C Schanen, S W Scherer, L C Tsui, U Francke. Cytogenet Cell Genet 1996
N C Schanen, S W Scherer, L C Tsui, U Francke. Cytogenet Cell Genet 1996
16
Familial chromosome translocation t(3;18)(p21;p11).
G Buchinger, A Wettstein, H Metze. J Med Genet 1981
G Buchinger, A Wettstein, H Metze. J Med Genet 1981
18
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
12
Criteria for the prenatal diagnosis of holoprosencephaly.
G Pilu, R Romero, N Rizzo, P Jeanty, L Bovicelli, J C Hobbins. Am J Perinatol 1987
G Pilu, R Romero, N Rizzo, P Jeanty, L Bovicelli, J C Hobbins. Am J Perinatol 1987
12
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.