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4. Semilobar holoprosencephaly with 21q22 deletion: an autopsy report. Mallick S; Panda SS; Ray R; Shukla R; Kabra M; Agarwal R BMJ Case Rep; 2014 Mar; 2014():. PubMed ID: 24626384 [TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of pure partial monosomy 18p associated with holoprosencephaly and congenital heart defects. Yi Z; Yingjun X; Yongzhen C; Liangying Z; Meijiao S; Baojiang C Gene; 2014 Jan; 533(2):565-9. PubMed ID: 24091065 [TBL] [Abstract][Full Text] [Related]
6. Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation. McCormack WM; Shen JJ; Curry SM; Berend SA; Kashork C; Pinar H; Potocki L; Bejjani BA Am J Med Genet; 2002 Nov; 112(4):384-9. PubMed ID: 12376941 [TBL] [Abstract][Full Text] [Related]
7. Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly. Hu T; Kruszka P; Martinez AF; Ming JE; Shabason EK; Raam MS; Shaikh TH; Pineda-Alvarez DE; Muenke M Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):175-186. PubMed ID: 30182442 [TBL] [Abstract][Full Text] [Related]
8. Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation. McCormack WM; Shen JJ; Curry SM; Berend SA; Kashork C; Pinar H; Potocki L; Bejjani BA Am J Med Genet A; 2003 Apr; 118A(2):384-9. PubMed ID: 12698964 [TBL] [Abstract][Full Text] [Related]
9. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes. Grammatico P; Majore S; Marrocco G; Poscente M; Mordenti C; Grammatico B; Del Porto G Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922 [TBL] [Abstract][Full Text] [Related]
10. Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q. Vance GH; Nickerson C; Sarnat L; Zhang A; Henegariu O; Morichon-Delvallez N; Butler MG; Palmer CG Am J Med Genet; 1998 Feb; 76(1):51-7. PubMed ID: 9508065 [TBL] [Abstract][Full Text] [Related]
11. Forebrain cleavage gene causing holoprosencephaly: deletion mapping to chromosome band 2p21. Hecht BK; Hecht F; Münke M Am J Med Genet; 1991 Jul; 40(1):130. PubMed ID: 1887845 [No Abstract] [Full Text] [Related]
12. Holoprosencephaly: An update on cytogenetic abnormalities. Bendavid C; Dupé V; Rochard L; Gicquel I; Dubourg C; David V Am J Med Genet C Semin Med Genet; 2010 Feb; 154C(1):86-92. PubMed ID: 20104602 [TBL] [Abstract][Full Text] [Related]
13. Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotype. Kanafani S; Aboura A; Pipiras E; Carbillon L; Tabet AC; Largillière C; Garel C; Gressens P; Bucourt M; Cedrin-Durnerin I; Lachassinne E; Roumegoux C; Uzan M; Hugues JN; Wolf JP; Benzacken B Prenat Diagn; 2007 Mar; 27(3):279-84. PubMed ID: 17269127 [TBL] [Abstract][Full Text] [Related]
14. [One case of 2q37 deletion syndrome: clinical and genetic diagnosis]. Geng Q; Xie JS; Wu WQ; Luo FW; Chen WB Zhonghua Er Ke Za Zhi; 2013 Dec; 51(12):934-7. PubMed ID: 24495766 [TBL] [Abstract][Full Text] [Related]
15. Holoprosencephaly due to numeric chromosome abnormalities. Solomon BD; Rosenbaum KN; Meck JM; Muenke M Am J Med Genet C Semin Med Genet; 2010 Feb; 154C(1):146-8. PubMed ID: 20104610 [TBL] [Abstract][Full Text] [Related]
16. Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3). Estabrooks LL; Rao KW; Donahue RP; Aylsworth AS Am J Med Genet; 1990 Jul; 36(3):306-9. PubMed ID: 2363428 [TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly? Karmous-Benailly H; Tabet AC; Thaly A; Dupuy O; Huten Y; Luton D; Baumann C; Delezoide AL Prenat Diagn; 2005 Mar; 25(3):193-7. PubMed ID: 15791668 [TBL] [Abstract][Full Text] [Related]
18. Physical mapping of the holoprosencephaly critical region in 18p11.3. Overhauser J; Mitchell HF; Zackai EH; Tick DB; Rojas K; Muenke M Am J Hum Genet; 1995 Nov; 57(5):1080-5. PubMed ID: 7485158 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly. Chen CP; Kuo YK; Su YN; Chern SR; Tsai FJ; Wu PC; Chen YT; Town DD; Wang W Taiwan J Obstet Gynecol; 2011 Jun; 50(2):182-7. PubMed ID: 21791305 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]