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.
44. Basic genetic concepts for the orthopedic surgeon. Pashayan HM Orthop Clin North Am; 1976 Apr; 7(2):265-80. PubMed ID: 131283 [No Abstract] [Full Text] [Related]
45. Antenatal genetic diagnosis in a kindred with a 15p plus chromosome. Hahnemann N; Eiberg H Clin Genet; 1973 Jun; 4(6):464-73. PubMed ID: 4132613 [No Abstract] [Full Text] [Related]
46. Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes. Flori E; Biancalana V; Girard-Lemaire F; Favre R; Flori J; Doray B; Mandel JL Eur J Hum Genet; 2004 Mar; 12(3):181-6. PubMed ID: 14694357 [TBL] [Abstract][Full Text] [Related]
47. [Partial trisomy 13 for the distal long arm and its prenatal diagnosis]. Zolotukhina TV; Rozovskiĭ IS; Bartseva OB; Vakhlamova IV; Bubnova NI Genetika; 1982 Nov; 18(11):1899-905. PubMed ID: 6891355 [TBL] [Abstract][Full Text] [Related]
48. Chromosome studies in abnormal children. Rahimtoola R; Qureshi HB; Naz S; Majid I J Pak Med Assoc; 1975 Jun; 25(6):124-9. PubMed ID: 129579 [No Abstract] [Full Text] [Related]
49. Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements. Soler A; Margarit E; Carrió A; Costa D; Queralt R; Ballesta F J Med Genet; 1999 Apr; 36(4):333-4. PubMed ID: 10227405 [TBL] [Abstract][Full Text] [Related]
50. Abnormal chromosome 18 in prenatal diagnosis with holoprosencephaly. de Pater JM; Scheres JM; Brons J Prenat Diagn; 1997 Sep; 17(9):887-8. PubMed ID: 9316141 [No Abstract] [Full Text] [Related]
51. Approaches to the prenatal diagnosis of the Prader-Willi syndrome. Schinzel A Hum Genet; 1986 Nov; 74(3):327. PubMed ID: 3781563 [No Abstract] [Full Text] [Related]
52. Cytogenetic studies on humans: some population aspects. Brown WM Proc R Soc Med; 1968 Feb; 61(2):164-7. PubMed ID: 4230058 [No Abstract] [Full Text] [Related]
53. [Late prenatal diagnosis of fetal growth retardation: the diagnosis of a case of trisomy 18 (author's transl)]. Le Marec B; Defawe G; Mention JE; Picard F; Duval JM; Dubois J J Gynecol Obstet Biol Reprod (Paris); 1980; 9(6):655-7. PubMed ID: 7462570 [TBL] [Abstract][Full Text] [Related]
54. Sex ratios in fetuses and liveborn infants with autosomal aneuploidy. Huether CA; Martin RL; Stoppelman SM; D'Souza S; Bishop JK; Torfs CP; Lorey F; May KM; Hanna JS; Baird PA; Kelly JC Am J Med Genet; 1996 Jun; 63(3):492-500. PubMed ID: 8737659 [TBL] [Abstract][Full Text] [Related]
55. [Importance and trends of prenatal diagnostics]. Sandig KR; Mücke J; Theile H Z Gesamte Inn Med; 1981 Jun; 36(11):352-6. PubMed ID: 7303761 [TBL] [Abstract][Full Text] [Related]
56. [Chromosome aberrations in children from endangered pregnancies]. Goetz P Cesk Pediatr; 1973 Jan; 28(1):12-6. PubMed ID: 4265430 [No Abstract] [Full Text] [Related]
58. An introduction to cytogenetics in medicine and dentistry. Lustenberger AA; Shapiro LR J Oral Med; 1974; 29(3):64-8. PubMed ID: 4276810 [No Abstract] [Full Text] [Related]
59. [Prader-Willi syndrome in a young infant]. Hack WW; ten Houten R; Breslau-Suderius EJ; Halley DJ Ned Tijdschr Geneeskd; 1997 Oct; 141(42):2025-8. PubMed ID: 9550755 [TBL] [Abstract][Full Text] [Related]
60. Prenatal diagnosis of a 5/15 translocation with 5p and proximal 5q trisomy. Cytogenetic and phenotypic findings. Crowder WE; Yeast JD; Falk RE Birth Defects Orig Artic Ser; 1982; 18(3 Pt A):143-51. PubMed ID: 7126787 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]