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43. Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX. Cremonini G; Poggi A; Capucci R; Vesce F; Patella A; Marci R J Obstet Gynaecol Res; 2014 Jan; 40(1):259-62. PubMed ID: 23937348 [TBL] [Abstract][Full Text] [Related]
44. Chromosome 13 long arm interstitial deletion associated with features of Noonan phenotype. Onufer CN; Stephan MJ; Thuline HC; Char F Ann Genet; 1987; 30(4):236-9. PubMed ID: 3501267 [TBL] [Abstract][Full Text] [Related]
45. [THE NOSOLOGY OF SO-CALLED MALE TURNER'S SYNDROME]. OVERZIER C Dtsch Arch Klin Med; 1964 Mar; 209():422-44. PubMed ID: 14187126 [No Abstract] [Full Text] [Related]
46. Fetal therapy and cytogenetic testing: prenatal detection of chromosome aberration during thoracocentesis for congenital chylothorax by karyotyping from pleural effusion fluid and review of the literature. Chen CP Genet Couns; 2005; 16(3):301-5. PubMed ID: 16259328 [TBL] [Abstract][Full Text] [Related]
47. Jarcho-Levin syndrome: two consecutive pregnancies in a Puerto Rican couple. Wong G; Levine D Ultrasound Obstet Gynecol; 1998 Jul; 12(1):70-3. PubMed ID: 9697288 [TBL] [Abstract][Full Text] [Related]
48. Neurofibromatosis with fully expressed Noonan syndrome. Abuelo DN; Meryash DL Am J Med Genet; 1988 Apr; 29(4):937-41. PubMed ID: 3135755 [TBL] [Abstract][Full Text] [Related]
49. Molecular detection of a translocation (Y;15) in a 45,X male. Disteche CM; Brown L; Saal H; Friedman C; Thuline HC; Hoar DI; Pagon RA; Page DC Hum Genet; 1986 Dec; 74(4):372-7. PubMed ID: 3793100 [TBL] [Abstract][Full Text] [Related]
50. [Methodology of gene analysis and metabolic studies]. Moser H Arch Gynecol Obstet; 1992; 252 Suppl():S22-30. PubMed ID: 1482202 [No Abstract] [Full Text] [Related]
51. [Variability in clinical expression of Noonan syndrome--the report of two familial cases]. Klapecki J; Obersztyn E; Łaniewski-Wołłk M; Szpecht-Potocka A; Mazurczak T Wiad Lek; 2008; 61(1-3):74-81. PubMed ID: 18717048 [TBL] [Abstract][Full Text] [Related]
52. Genetic heterogeneity in Noonan syndrome: evidence for an autosomal recessive form. van Der Burgt I; Brunner H Am J Med Genet; 2000 Sep; 94(1):46-51. PubMed ID: 10982482 [TBL] [Abstract][Full Text] [Related]
53. Noonan syndrome or new autosomal dominant condition with coarctation of the aorta, hypertrophic cardiomyopathy, and minor anomalies. Lemire EG Am J Med Genet; 2002 Dec; 113(3):286-90. PubMed ID: 12439898 [TBL] [Abstract][Full Text] [Related]
54. Surfactant protein B deficiency: a rare but lethal condition in newborn. Acharyya S; Acharyya K Indian Pediatr; 2001 Sep; 38(9):1039-41. PubMed ID: 11568382 [No Abstract] [Full Text] [Related]