These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 37189898)

  • 1. Holoprosencephaly: Review of Embryology, Clinical Phenotypes, Etiology and Management.
    Malta M; AlMutiri R; Martin CS; Srour M
    Children (Basel); 2023 Mar; 10(4):. PubMed ID: 37189898
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Semilobar Holoprosencephaly: Capacious Anomaly in the Cephalad.
    Veluchamy M; Murugan M
    Cureus; 2020 Jul; 12(7):e9181. PubMed ID: 32802616
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
    Winter TC; Kennedy AM; Woodward PJ
    Radiographics; 2015; 35(1):275-90. PubMed ID: 25590404
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation.
    Hahn JS; Barnes PD
    Am J Med Genet C Semin Med Genet; 2010 Feb; 154C(1):120-32. PubMed ID: 20104607
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH Gene.
    Coutton C; Poreau B; Devillard F; Durand C; Odent S; Rozel C; Vieville G; Amblard F; Jouk PS; Satre V
    Mol Syndromol; 2014 Jan; 5(1):25-31. PubMed ID: 24550762
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Holoprosencephaly.
    Dubourg C; Bendavid C; Pasquier L; Henry C; Odent S; David V
    Orphanet J Rare Dis; 2007 Feb; 2():8. PubMed ID: 17274816
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
    Roessler E; Belloni E; Gaudenz K; Jay P; Berta P; Scherer SW; Tsui LC; Muenke M
    Nat Genet; 1996 Nov; 14(3):357-60. PubMed ID: 8896572
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects.
    Dennis JF; Kurosaka H; Iulianella A; Pace J; Thomas N; Beckham S; Williams T; Trainor PA
    PLoS Genet; 2012; 8(10):e1002927. PubMed ID: 23055936
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Boc modifies the holoprosencephaly spectrum of Cdo mutant mice.
    Zhang W; Hong M; Bae GU; Kang JS; Krauss RS
    Dis Model Mech; 2011 May; 4(3):368-80. PubMed ID: 21183473
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expression of the Sonic hedgehog (SHH ) gene during early human development and phenotypic expression of new mutations causing holoprosencephaly.
    Odent S; Atti-Bitach T; Blayau M; Mathieu M; Aug J; Delezo de AL; Gall JY; Le Marec B; Munnich A; David V; Vekemans M
    Hum Mol Genet; 1999 Sep; 8(9):1683-9. PubMed ID: 10441331
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cdon mutation and fetal ethanol exposure synergize to produce midline signaling defects and holoprosencephaly spectrum disorders in mice.
    Hong M; Krauss RS
    PLoS Genet; 2012; 8(10):e1002999. PubMed ID: 23071453
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog.
    Solomon BD; Bear KA; Wyllie A; Keaton AA; Dubourg C; David V; Mercier S; Odent S; Hehr U; Paulussen A; Clegg NJ; Delgado MR; Bale SJ; Lacbawan F; Ardinger HH; Aylsworth AS; Bhengu NL; Braddock S; Brookhyser K; Burton B; Gaspar H; Grix A; Horovitz D; Kanetzke E; Kayserili H; Lev D; Nikkel SM; Norton M; Roberts R; Saal H; Schaefer GB; Schneider A; Smith EK; Sowry E; Spence MA; Shalev SA; Steiner CE; Thompson EM; Winder TL; Balog JZ; Hadley DW; Zhou N; Pineda-Alvarez DE; Roessler E; Muenke M
    J Med Genet; 2012 Jul; 49(7):473-9. PubMed ID: 22791840
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Modeling the complex etiology of holoprosencephaly in mice.
    Hong M; Krauss RS
    Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):140-150. PubMed ID: 29749693
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Extreme variability of expression of a Sonic Hedgehog mutation: attention difficulties and holoprosencephaly.
    Heussler HS; Suri M; Young ID; Muenke M
    Arch Dis Child; 2002 Apr; 86(4):293-6. PubMed ID: 11919111
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Holoprosencephaly: from Homer to Hedgehog.
    Ming JE; Muenke M
    Clin Genet; 1998 Mar; 53(3):155-63. PubMed ID: 9630065
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations.
    El-Dessouky SH; Aboulghar MM; Gaafar HM; Abdella RM; Sharaf MF; Ateya MI; Elarab AE; Zidan WH; Helal RM; Aboelsaud SM; Eid MM; Abdel-Salam GMH
    Prenat Diagn; 2020 Apr; 40(5):565-576. PubMed ID: 31955448
    [TBL] [Abstract][Full Text] [Related]  

  • 17. New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
    Mercier S; Dubourg C; Garcelon N; Campillo-Gimenez B; Gicquel I; Belleguic M; Ratié L; Pasquier L; Loget P; Bendavid C; Jaillard S; Rochard L; Quélin C; Dupé V; David V; Odent S
    J Med Genet; 2011 Nov; 48(11):752-60. PubMed ID: 21940735
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
    Nanni L; Ming JE; Bocian M; Steinhaus K; Bianchi DW; Die-Smulders C; Giannotti A; Imaizumi K; Jones KL; Campo MD; Martin RA; Meinecke P; Pierpont ME; Robin NH; Young ID; Roessler E; Muenke M
    Hum Mol Genet; 1999 Dec; 8(13):2479-88. PubMed ID: 10556296
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.