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 *

71 related articles for article (PubMed ID: 2973235)

  • 41. [20 cases of trisomy 18. Sex-ratio in relation to age of the mother].
    Le Marec BM; Lair JC; Kérisit J; Le Mée F; Sénécal J
    Ann Pediatr (Paris); 1977 Feb; 24(2):125-36. PubMed ID: 16211953
    [No Abstract]   [Full Text] [Related]  

  • 42. [Genetic study of children with congenital heart defects].
    Fäller K; Szollár J
    Orv Hetil; 1984 Aug; 125(34):2071-5. PubMed ID: 6237297
    [No Abstract]   [Full Text] [Related]  

  • 43. Duplication 3p21----3pter and cyclopia.
    Kurtzman DN; Van Dyke DL; Rich CA; Weiss L
    Am J Med Genet; 1987 May; 27(1):33-7. PubMed ID: 3605204
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions.
    Sebastio G; Perone L; Guzzetta V; Sebastio L; Vicari L; Della Casa R; Gurrieri F; Zappata S; Pomponi MG; Mazzei A; Neri G; Andria G; Brahe C
    Am J Med Genet; 1996 May; 63(2):366-72. PubMed ID: 8725787
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Anorectal malformation and Down's syndrome in monozygotic twins.
    de Buys Roessingh AS; Mueller C; Wiesenauer C; Bensoussan AL; Beaunoyer M
    J Pediatr Surg; 2009 Feb; 44(2):e13-6. PubMed ID: 19231514
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Sub-band deletion of 7q36.3 in a patient with ring chromosome 7: association with holoprosencephaly.
    Sawyer JR; Lukacs JL; Hassed SJ; Arnold GL; Mitchell HF; Muenke M
    Am J Med Genet; 1996 Oct; 65(2):113-6. PubMed ID: 8911601
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Coexistence of congenital heart defects with other congenital abnormalities].
    Ostapiuk H; Sobaniec-Lotowska M; Sulkowski S; Ostapiuk W; Famulski W
    Wiad Lek; 1988 May; 41(9):550-3. PubMed ID: 2977024
    [No Abstract]   [Full Text] [Related]  

  • 48. Familial agnathia-holoprosencephaly.
    Pauli RM; Pettersen JC; Arya S; Gilbert EF
    Am J Med Genet; 1983 Apr; 14(4):677-98. PubMed ID: 6846401
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Genetic counseling in neurosurgical diseases (author's transl)].
    Takeshita K
    No Shinkei Geka; 1980 Mar; 8(3):211-9. PubMed ID: 6445514
    [No Abstract]   [Full Text] [Related]  

  • 50. 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]  

  • 51. [Clinical and pathological studies in 3 cases of holoprosencephaly].
    Kumagai K; Seki Y; Goto N
    Shinkei Kenkyu No Shimpo; 1972 Apr; 16(2):293-301. PubMed ID: 5063789
    [No Abstract]   [Full Text] [Related]  

  • 52. [Abnormalities associated with Down's syndrome. Observations on 404 cases observed in Italy between 1960 and 1966].
    Ceccarelli G; Torbidoni L
    Pediatria (Napoli); 1968 Oct; 76(5):708-17. PubMed ID: 4243795
    [No Abstract]   [Full Text] [Related]  

  • 53. [Perinatal leukemia].
    Stransky E
    Arch Kinderheilkd; 1968; 178(1):8-18. PubMed ID: 4238056
    [No Abstract]   [Full Text] [Related]  

  • 54. [Indentification of chromosomal polymorphisms and some aberrations identified by new cytogenetical methods (author's transl)].
    Kunze J; Tolksdorf M
    Z Kinderheilkd; 1974 Apr; 117(1):29-46. PubMed ID: 4275663
    [No Abstract]   [Full Text] [Related]  

  • 55. Syndromes associated with holoprosencephaly.
    Kruszka P; Muenke M
    Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):229-237. PubMed ID: 29770994
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. Chance vs. causality in the association of Down syndrome and holoprosencephaly.
    Epstein CJ; Seto S; Golabi M
    Am J Med Genet; 1988 Aug; 30(4):939-42. PubMed ID: 2973235
    [No Abstract]   [Full Text] [Related]  

  • 58. Association of holoprosencephaly and Down syndrome.
    Martinez-Frías ML
    Am J Med Genet; 1989 Mar; 32(3):435. PubMed ID: 2524971
    [No Abstract]   [Full Text] [Related]  

  • 59. Holoprosencephaly and trisomy 21 in a child born to a nondiabetic mother.
    Urioste M; Valcarcel E; Gomez MA; Pinel I; Garcia de León R; Diaz de Bustamante A; Tebar R; Martinez-Frias ML
    Am J Med Genet; 1988 Aug; 30(4):925-8. PubMed ID: 2973234
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Holoprosencephaly in a Down syndrome child.
    Pi SY; Fineman RM; Wing SD; Grunnet M; Chan G
    Am J Med Genet; 1980; 5(2):201-6. PubMed ID: 6446857
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.