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 *

73 related articles for article (PubMed ID: 2817005)

  • 1. XK aprosencephaly may be a new mutation or a dominant genetic defect.
    Benke PJ
    Am J Med Genet; 1989 Oct; 34(2):250-1. PubMed ID: 2817005
    [No Abstract]   [Full Text] [Related]  

  • 2. Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome.
    Lurie IW; Nedzved MK; Lazjuk GI; Kirillova IA; Cherstvoy ED
    Am J Med Genet; 1979; 3(3):301-9. PubMed ID: 114053
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant inheritance of the DeMyer Sequence.
    Jaramillo C; Brandt SK; Jorgenson RJ
    J Craniofac Genet Dev Biol; 1988; 8(3):199-204. PubMed ID: 3209682
    [TBL] [Abstract][Full Text] [Related]  

  • 4. XK aprosencephaly and anencephaly in sibs.
    Townes PL; Reuter K; Rosquete EE; Magee BD
    Am J Med Genet; 1988 Mar; 29(3):523-8. PubMed ID: 3287923
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mosaic r(13) in an infant with aprosencephaly.
    Goldsmith CL; Tawagi GF; Carpenter BF; Speevak MD; Hunter AG
    Am J Med Genet; 1993 Sep; 47(4):531-3. PubMed ID: 8256818
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities.
    Cohen MM
    Am J Med Genet; 1989 Oct; 34(2):271-88. PubMed ID: 2683788
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new syndrome with distinct facial and auricular malformations and dominant inheritance.
    Simosa V; Penchaszadeh VB; Bustos T
    Am J Med Genet; 1989 Feb; 32(2):184-6. PubMed ID: 2929657
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Fatal genetic-morphologic syndromes. The campomelic syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 May; 14(3):162-4. PubMed ID: 8516273
    [No Abstract]   [Full Text] [Related]  

  • 9. [Genetic-morphologic fatal syndromes. Cerebro-oculo-facioskeletal syndrome (Pena-Shokeir syndrome II)].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Jul; 14(4):219-20. PubMed ID: 8367388
    [No Abstract]   [Full Text] [Related]  

  • 10. The XK-aprosencephaly syndrome.
    Lurie IW; Nedzed MK; Lazjuk GI; Kirillova IA; Cherstvoy ED; Ostrovskaja TI; Shved IA
    Am J Med Genet; 1980; 7(2):231-4. PubMed ID: 7193413
    [No Abstract]   [Full Text] [Related]  

  • 11. SHORT syndrome: a new case with probable autosomal dominant inheritance.
    Sorge G; Ruggieri M; Polizzi A; Scuderi A; Di Pietro M
    Am J Med Genet; 1996 Jan; 61(2):178-81. PubMed ID: 8669449
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic-morphologic fatal syndromes. Fetal akinesia sequence (Pena-Shokeir syndrome I)].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Jul; 14(4):216-8. PubMed ID: 8367387
    [No Abstract]   [Full Text] [Related]  

  • 13. Teebi hypertelorism syndrome: report of a third family.
    Toriello HV; Delp K
    Clin Dysmorphol; 1994 Oct; 3(4):335-9. PubMed ID: 7894738
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genetic morphologic fatal syndromes. Neu-Laxova syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Sep; 14(5):271-3. PubMed ID: 8415438
    [No Abstract]   [Full Text] [Related]  

  • 15. [Anesthesia in Sotos' syndrome].
    de Nadal M; Hervás C; Trull T; Saludes J; Miguel E
    Rev Esp Anestesiol Reanim; 1993; 40(6):375-6. PubMed ID: 8134682
    [No Abstract]   [Full Text] [Related]  

  • 16. [Facial hemihyperplasia associated with strabismus inherited by dominant trait].
    Bencze J; Schnitzler A; Walawska J
    Orv Hetil; 1972 Sep; 113(36):2172-5. PubMed ID: 5051104
    [No Abstract]   [Full Text] [Related]  

  • 17. Absence of fibula and ulna with oligodactyly, contractures, right-angle bowing of femora, abnormal facial morphology, cleft lip/palate and brain malformation in two sibs: a possibly new lethal syndrome.
    Pfeiffer RA; Stöss H; Voight HJ; Wündisch GF
    Am J Med Genet; 1988 Apr; 29(4):901-8. PubMed ID: 3400735
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Interference with gastrulation during the third week of pregnancy as a cause of some facial abnormalities and CNS defects.
    Webster WS; Lipson AH; Sulik KK
    Am J Med Genet; 1988 Nov; 31(3):505-12. PubMed ID: 3067574
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Apple peel atresia in association with bilateral colobomatous malformation of the optic nerve heads, dysmorphic features, and learning disability - a new syndrome?
    Waters FM; Lloyd IC; Clayton-Smith J
    Ophthalmic Genet; 2000 Jun; 21(2):117-21. PubMed ID: 10916186
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?
    Seller MJ; Pal K; Moscoso G; Nicolaides K; Hyett JA
    Clin Dysmorphol; 1998 Jan; 7(1):41-4. PubMed ID: 9546829
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.