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 *

129 related articles for article (PubMed ID: 9747372)

  • 21. A rare case of aplasia cutis congenita with refractory seizures.
    Wu PC; Jiang JP; Wang CC; Chen SJ
    Pediatr Neurol; 2008 Dec; 39(6):435-7. PubMed ID: 19027593
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A case of focal facial dermal dysplasia type 4.
    Mehrtens SH; Shankar S
    Pediatr Dermatol; 2019 Jan; 36(1):e58-e59. PubMed ID: 30561078
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Aplasia cutis congenita.
    Chitkara AJ; Anand NK; Saini L
    Indian Pediatr; 1985 Jan; 22(1):69-71. PubMed ID: 3841089
    [No Abstract]   [Full Text] [Related]  

  • 24. Epidermal naevi and bullous aplasia cutis congenita in a neonate.
    Fryburg JS; Greer KE
    J Med Genet; 1993 Nov; 30(11):962-3. PubMed ID: 8301655
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Aplasia cutis congenita in a premature infant].
    Rasmussen HH; Vissing IS; Skov M
    Ugeskr Laeger; 1996 Jun; 158(24):3472-4. PubMed ID: 8650819
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Aplasia cutis congenita associated with Goltz syndrome in a male neonate.
    Gnamey DK; Koffi KS; Nagalo K; Guedenon KM; Akakpo-Numado GK; Balaka B; Tatagan-Agbi K; Atakouma DY
    Genet Couns; 2010; 21(1):41-7. PubMed ID: 20420028
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation.
    Yağci-Küpeli B; Çağlar K; Büyük S; Balci S
    Genet Couns; 2011; 22(1):55-61. PubMed ID: 21614989
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A case of systemic aplasia cutis congenita: a newly recognized syndrome?
    Sugiura T; Kouwaki M; Kiyosawa S; Sasada Y; Maeda M; Goto K; Koyama N
    Eur J Pediatr; 2008 Apr; 167(4):409-13. PubMed ID: 17520283
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome.
    Wimplinger I; Rauch A; Orth U; Schwarzer U; Trautmann U; Kutsche K
    Eur J Med Genet; 2007; 50(6):421-31. PubMed ID: 17845869
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Focal preauricular dermal dysplasia: report of two cases and a review of literature.
    Krathen MS; Rosenbach M; Yan AC; Crawford GH
    Pediatr Dermatol; 2008; 25(3):344-8. PubMed ID: 18577040
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Aplasia cutis congenita of the vertex in the newborn].
    Abilkassem R; Agadr A
    Pan Afr Med J; 2013; 16():148. PubMed ID: 24876906
    [No Abstract]   [Full Text] [Related]  

  • 32. A case of extensive aplasia cutis congenita: a conservative approach.
    Starcevic M; Sepec MP; Zah V
    Pediatr Dermatol; 2010; 27(5):540-2. PubMed ID: 20807357
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome?
    Naritomi K; Izumikawa Y; Nagataki S; Fukushima Y; Wakui K; Niikawa N; Hirayama K
    Am J Med Genet; 1992 Jul; 43(5):839-43. PubMed ID: 1642272
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Multiple congenital facial papules--quiz case. Multiple accessory tragi and aplasia cutis congenita in association with Delleman (oculocerebrocutaneous) syndrome.
    Agim NG; Hunt CM; Williams VL; Metry DW
    Arch Dermatol; 2011 Mar; 147(3):345-50. PubMed ID: 21422346
    [No Abstract]   [Full Text] [Related]  

  • 35. Aplasia Cutis Congenita in a Newborn Child Associated with Two Fetus Papyraceous.
    Šimić D; Prohić A; Puizina Ivić N; Zeljko Penavić J; Tomić T
    Acta Dermatovenerol Croat; 2015; 23(4):293-7. PubMed ID: 26724883
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Systemic aplasia cutis congenita: A case report and review of the literature.
    Zhou J; Zheng L; Tao W
    Pathol Res Pract; 2010 Jul; 206(7):504-7. PubMed ID: 20188489
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Abdominal aplasia cutis congenita: case report and review of the literature.
    Verhelle NA; Heymans O; Deleuze JP; Fabre G; Vranckx JJ; Van den hof B
    J Pediatr Surg; 2004 Feb; 39(2):237-9. PubMed ID: 14966752
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Aplasia cutis congenita: an association with vanishing twin syndrome.
    Maccario S; Fasolato V; Brunelli A; Martinelli S
    Eur J Dermatol; 2009; 19(4):372-4. PubMed ID: 19467960
    [TBL] [Abstract][Full Text] [Related]  

  • 39. De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies.
    Temple IK; Hurst JA; Hing S; Butler L; Baraitser M
    J Med Genet; 1990 Jan; 27(1):56-8. PubMed ID: 2308156
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Congenital cutaneous defects as complications in surviving co-twins. Aplasia cutis congenita and neonatal volkmann ischemic contracture of the forearm.
    Léauté-Labrèze C; Depaire-Duclos F; Sarlangue J; Fontan D; Sandler B; Maleville J; Taïeb A
    Arch Dermatol; 1998 Sep; 134(9):1121-4. PubMed ID: 9762026
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.