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 *

148 related articles for article (PubMed ID: 6854450)

  • 41. Bilateral femoral agenesis in femoral facial syndrome in a 19-week-old fetus.
    Campbell F; Vujanić GM
    Am J Med Genet; 1997 Oct; 72(3):315-8. PubMed ID: 9332661
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H): a model of a developmental field defect.
    Sorge G; Ardito S; Genuardi M; Pavone V; Rizzo R; Conti G; Neri G; Katz BE; Opitz JM
    Am J Med Genet; 1995 Feb; 55(4):427-32. PubMed ID: 7762582
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Variation in clinical and genitourinary lesions associated with pulmonary hypoplasia in Potter's syndrome--two autopsy reports.
    Jain M; Agarwal S; Mandal S
    Indian J Pathol Microbiol; 2006 Jul; 49(3):416-8. PubMed ID: 17001905
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and mental retardation: a new syndrome?
    Ramos-Arroyo MA; Clark GG; Saksena SS; Hodes ME
    Am J Med Genet; 1987 Feb; 26(2):345-54. PubMed ID: 2433942
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML; Pai GS; Wilkes B; Lebel RR
    Am J Med Genet; 2001 Aug; 102(3):237-42. PubMed ID: 11484200
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Airway management in a baby with femoral hypoplasia--unusual facies syndrome.
    Nguyen NH; Mayhew JF
    Paediatr Anaesth; 2003 Jan; 13(1):87. PubMed ID: 12535049
    [No Abstract]   [Full Text] [Related]  

  • 47. Prenatal diagnosis of femoral-facial syndrome: report of two cases.
    Silvas E; Rypens F; Jovanovic M; Delezoide AL; Patey N
    Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):770-3. PubMed ID: 24254654
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Abnormal facies, cleft palate, and generalized dysostosis: a lethal X-linked syndrome.
    André M; Vigneron J; Didier F
    J Pediatr; 1981 May; 98(5):747-52. PubMed ID: 7229752
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG; Reed SD; Rosenbaum KN; Gershanik J; Chen H; Wilson KM
    Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome.
    Chen H; Immken L; Lachman R; Yang S; Rimoin DL; Rightmire D; Eteson D; Stewart F; Beemer FA; Opitz JM
    Am J Med Genet; 1984 Apr; 17(4):809-26. PubMed ID: 6720746
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Femoral-facial syndrome--prenatal diagnosis--autosomal dominant inheritance.
    Robinow M; Sonek J; Buttino L; Veghte A
    Am J Med Genet; 1995 Jul; 57(3):397-9. PubMed ID: 7677141
    [TBL] [Abstract][Full Text] [Related]  

  • 52. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE
    Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Femoral hypoplasia unusual facies syndrome with preaxial polydactyly.
    Baraitser M; Reardon W; Oley C; Fixsen J
    Clin Dysmorphol; 1994 Jan; 3(1):40-5. PubMed ID: 8205325
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Plantar lipomatosis, unusual facies, and developmental delay: confirmation of Pierpont syndrome.
    Oudesluijs GG; Hordijk R; Boon M; Sijens PE; Hennekam RC
    Am J Med Genet A; 2005 Aug; 137(1):77-80. PubMed ID: 16007632
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Two brothers with Burn-McKeown syndrome.
    Wieczorek D; Teber OA; Lohmann D; Gillessen-Kaesbach G
    Clin Dysmorphol; 2003 Jul; 12(3):171-4. PubMed ID: 14564154
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Femoral hypoplasia in two newborns associated with maternal diabetes mellitus.
    Buyukkayhan D; Koklu E; Akcakus M; Kurtoglu S
    J Pediatr Endocrinol Metab; 2007 Oct; 20(10):1151-4. PubMed ID: 18051935
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A new short rib syndrome: report of two cases.
    Beemer FA; Langer LO; Klep-de Pater JM; Hemmes AM; Bylsma JB; Pauli RM; Myers TL; Haws CC
    Am J Med Genet; 1983 Jan; 14(1):115-23. PubMed ID: 6829599
    [TBL] [Abstract][Full Text] [Related]  

  • 58. "Newer" facial clefting syndromes.
    Gorlin RJ; Cervenka J; Cohen MM
    Birth Defects Orig Artic Ser; 1977; 13(3B):1-9. PubMed ID: 329913
    [No Abstract]   [Full Text] [Related]  

  • 59. Char syndrome (unusual mouth, patent ductus arteriosus, phalangeal anomalies).
    Temple IK
    Clin Dysmorphol; 1992 Jan; 1(1):17-21. PubMed ID: 1342853
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Brief clinical report: femoral hypoplasia--unusual facies syndrome.
    Hurst D; Johnson DF
    Am J Med Genet; 1980; 5(3):255-8. PubMed ID: 7405957
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.