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 *

185 related articles for article (PubMed ID: 5994491)

  • 1. [On an unusual case of multiple congenital malformations].
    Cela G
    Minerva Pediatr; 1966 Sep; 18(27):1500-5. PubMed ID: 5994491
    [No Abstract]   [Full Text] [Related]  

  • 2. [The etiopathogenesis of congenital multiple malformations].
    D'Addato F; Visentin L; Surico N
    Minerva Ginecol; 1979 Sep; 31(9):639-44. PubMed ID: 43957
    [No Abstract]   [Full Text] [Related]  

  • 3. Amniotic band sequence: Streeter hypothesis revisited.
    Bamforth JS
    Birth Defects Orig Artic Ser; 1993; 29(1):279-89. PubMed ID: 8280880
    [No Abstract]   [Full Text] [Related]  

  • 4. Potter's syndrome: bilateral renal agenesis (a report of two cases emphasizing associated malformations).
    Tinaztepe K; Balci S; Tinaztepe B; Dağli E
    Turk J Pediatr; 1983; 25(3):179-87. PubMed ID: 6673215
    [No Abstract]   [Full Text] [Related]  

  • 5. [Low cholesterol and pathological manifestations: Smith-Lemli-Opitz syndrome].
    Franceschini P; Franceschini D
    Minerva Pediatr; 1994 Dec; 46(12):579-80. PubMed ID: 7731422
    [No Abstract]   [Full Text] [Related]  

  • 6. [Anatomopathological aspects as risk factors in esophageal atresia].
    Fufezan V; Duică C; Socoliuc M; Sberea E; Corneanu A; Tepeneu P
    Rev Pediatr Obstet Ginecol Pediatr; 1980; 29(3):247-54. PubMed ID: 6781033
    [No Abstract]   [Full Text] [Related]  

  • 7. [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]  

  • 8. [On a case of grave congenital multiple malformations].
    Capra Marzani P; Guaschino S
    Minerva Pediatr; 1966 Nov; 18(33):1951-4. PubMed ID: 4232009
    [No Abstract]   [Full Text] [Related]  

  • 9. Otocephaly, and pulmonary malformation association: two case reports.
    Puvabanditsin S; Garrow E; Umaru S; Padilla J; Chowdawarapu S; Biswas A
    Genet Couns; 2006; 17(2):167-71. PubMed ID: 16970034
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Triploidy syndrome and diploid/triploid mixoploidy syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):361-2. PubMed ID: 11057261
    [No Abstract]   [Full Text] [Related]  

  • 11. [Skeletal changes in a case of unusual chromosome aberration. (Patient with chromosome complex 48, XXXX-49, XXXXX: comparison with the syndrome 49,XXXXY].
    Dallapiccola B; Pistocchi GF
    Radiol Med; 1968 Aug; 54(8):737-50. PubMed ID: 5190487
    [No Abstract]   [Full Text] [Related]  

  • 12. [Hemifacial microsomia. Description of a case with associated rare multiple visceral anomalies].
    Lapetina F; Romano A; Teza F; Piantoni G
    Pediatr Med Chir; 1985; 7(3):467-70. PubMed ID: 3837211
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two cases of severe lethal Smith-Lemli-Opitz syndrome.
    Belmont JW; Hawkins E; Hejtmancik JF; Greenberg F
    Am J Med Genet; 1987 Jan; 26(1):65-7. PubMed ID: 3812579
    [No Abstract]   [Full Text] [Related]  

  • 14. [Statistical study of congenital malformations at the Institute of Pathology of the University of Milan during 1946-66].
    Fundarò P; Rescaldani R; Puccetti U; Bratina G; Grigolato P
    Folia Hered Pathol (Milano); 1968; ():89-111. PubMed ID: 5760558
    [No Abstract]   [Full Text] [Related]  

  • 15. [On the importance of the absence of anumbilical artery and the possible consequences for fetal development].
    Justus B; Geissler U
    Z Arztl Fortbild (Jena); 1969 Feb; 63(3):140-3. PubMed ID: 5785462
    [No Abstract]   [Full Text] [Related]  

  • 16. [Urgency of surgical interventions in congenital deformities].
    Schober KL
    Z Arztl Fortbild (Jena); 1965 Apr; 59(7):364-7. PubMed ID: 5887269
    [No Abstract]   [Full Text] [Related]  

  • 17. A review and case report of aprosencephaly and the XK aprosencephaly syndrome.
    Martin RA; Carey JG
    Am J Med Genet; 1982 Mar; 11(3):369-71. PubMed ID: 7081301
    [No Abstract]   [Full Text] [Related]  

  • 18. [Autopsy case of endocardial fibroelastosis associated with multiple cardiac malformations and congenital pulmonary lymphangiectasis].
    Kaneko H; Okamura A
    Kyobu Geka; 1972 Feb; 25(2):121-7. PubMed ID: 5063449
    [No Abstract]   [Full Text] [Related]  

  • 19. [Multiple congenital malformations in a boy with a chromosome abnormality of the group F (46-XY, 20-P), the son of a clinically healthy subject with an analogous chromosome malformation].
    Loiodice G; Rovetta DG; Bellicini G; Callura G; Bergamo F
    Minerva Pediatr; 1970 May; 22(21):1084-8. PubMed ID: 4394837
    [No Abstract]   [Full Text] [Related]  

  • 20. Congenital cervical herniation of the lung. Report of a case.
    Stearman MD; Majd M; Lopresti JM
    Med Ann Dist Columbia; 1971 Dec; 40(12):759-60. PubMed ID: 4332620
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.