HaroldN.BassMDFACMG

PubMed

• 13 citations
  A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity
  Kavita S. Reddy, Swaroop Aradhya, Jeanne Meck, George E. Tiller, Sridevi Abboy, Harold N. Bass> ;Genetics in Medicine. 2013 Jan 1
• 9 citations
  Oligoarray (105K) CGH Analysis of Chromosome Microdeletions within 10q22.1q24.32
  K. S. Reddy, Rebecca Mardach, Harold N. Bass> ;Cytogenetic and Genome Research. 2011 Jan 1
• 15 citations
  Application of oligonucleotide array CGH to the simultaneous detection of a deletion in the nuclear TK2 gene and mtDNA depletion.
  Shulin Zhang, Fang yuan Li, Harold N. Bass, Amber Pursley, Eric S. Schmitt, Blaire L. Brown, Ellen K. Brundage, Rebecca Mardach, Lee-Jun C. Wong> ;Molecular Genetics and Metabolism. 2010 Jan 1
• 3 citations
  A pseudo-full mutation identified in fragile X assay reveals a novel base change abolishing an EcoRI restriction site.
  Shujian Liang, Harold N. Bass, Hanlin Gao, Caroline Astbury, Mehdi R. Jamehdor, Yong Qu> ;The Journal of Molecular Diagnostics. 2008 Sep 1
• 24 citations
  Trisomy 18 mosaicism: Clues to the diagnosis
  Harold N. Bass, Michelle Fox, Eric A. Wulfsberg, Robert S. Sparkes, BarbaraF. Crandall> ;Clinical Genetics. 2008 Apr 23
• 18 citations
  Neonatal Asymmetric Crying Facies: A New Look at an Old Problem:
  Samuel O. Sapin, Alvin A. Miller, Harold N. Bass> ;Clinical Pediatrics. 2005 Mar 1
• 71 citations
  Genetic counseling gone awry: miscommunication between prenatal genetic service providers and Mexican-origin clients.
  Carole H. Browner, H. Mabel Preloran, Maria Casado, Harold N. Bass, Ann P. Walker> ;Social Science & Medicine. 2003 May 1
• 6 citations
  Perinatal Screening for Congenital Malformations and Genetic Disorders: Current Status and Future Directions.
  Harold N. Bass, Jamie Beavers Taylor> ;The Permanente Journal. 2002 Jan 1
• 11 citations
  Spontaneous pneumothorax in association with pyridoxine-responsive homocystinuria
  Harold N. Bass, D. LaGrave, Rebecca Mardach, Stephen D. Cederbaum, C. D. Fuster, M. Chetty> ;Journal of Inherited Metabolic Disease. 1997 Nov 1
• 43 citations
  PCR-based screening for cystic fibrosis carrier mutations in an ethnically diverse pregnant population.
  Wayne W. Grody, Christine Dunkel-Schetter, Z H Tatsugawa, Michelle Fox, Carolyn Y. Fang, Rita M. Cantor, Jessica M. Novak, Harold N. Bass, Barbara F. Crandall> ;American Journal of Human Genetics. 1997 Apr 1
• 21 citations
  Attitudes toward genetic carrier screening for cystic fibrosis among pregnant women: the role of health beliefs and avoidant coping style.
  Carolyn Y. Fang, Christine Dunkel-Schetter, Z H Tatsugawa, Michelle Fox, Harold N. Bass, Barbara F. Crandall, Wayne W. Grody> ;Women's Health. 1997 Jan 1
• 22 citations
  Miller-Dieker Syndrome: Detection of a Cryptic Chromosome Translocation Using In Situ Hybridization in a Family With Multiple Affected Offspring
  Monica Alvarado, Harold N. Bass, Sibylle Caldwell, Mehdi R. Jamehdor, Alvin A. Miller, Peter Jacob> ;American Journal of Diseases of Children. 1993 Dec 1
• 20 citations
  Michelin tire baby syndrome: familial constriction bands during infancy and early childhood in four generations.
  Harold N. Bass, Sibylle Caldwell, Barry S. Brooks> ;American Journal of Medical Genetics. 1993 Feb 1
• 2 citations
  Association of generalized dystrophic epidermolysis bullosa with positive acetylcholinesterase and markedly elevated maternal serum and amniotic fluid alpha-fetoprotein
  Harold N. Bass, Cheryl Miranda, Rudolph Oei, Barbara F. Crandall> ;Prenatal Diagnosis. 1993 Jan 1
• 13 citations
  Churg-Strauss Syndrome in a 14-Year-Old Boy Diagnosed by Transbronchial Lung Biopsy
  Paul Treitman, Harold N. Bass, Joel L. Herskowitz> ;Clinical Pediatrics. 1991 Aug 1
• 22 citations
  Persistently elevated AFP and AChE in amniotic fluid from a normal fetus following demise of its twin
  Harold N. Bass, Joan B. Oliver, Murali Srinivasan, Ruth Petrucha, Won G. Ng, Jo Ellen S. Lee> ;Prenatal Diagnosis. 1986 Jan 1
• Evidence from somatic cells for crossing-over in humans
  R. S. Sparkes, M.C. Sparkes, Harold N. Bass> ;Cytogenetics and Cell Genetics. 1986 Jan 1
• 20 citations
  Congenital contractural arachnodactyly, keratoconus, and probable Marfan syndrome in the same pedigree
  Harold N. Bass, Robert S. Sparkes, Barbara F. Crandall, S. Michael Marcy> ;The Journal of Pediatrics. 1981 Apr 1
• 18 citations
  Osteopathia Striata Syndrome Clinical, Genetic and Radiologic Considerations
  Harold N. Bass, Jay R. Weiner, Alan Goldman, Lorraine E. Smith, Robert S. Sparkes, Barbara F. Crandall> ;Clinical Pediatrics. 1980 May 1
• 23 citations
  Features of trisomy 18 and 18p- syndromes in an infant with 45,XY,i(18q).
  Harold N. Bass, Robert S. Sparkes, Alvin A. Miller> ;Clinical Genetics. 2008 Apr 23
• 6 citations
  10q(q23→qter) duplication: GOTs, HK1, and other gene markers
  Robert S. Sparkes, Harold N. Bass, Maryellen C. Sparkes> ;Human Genetics. 1978 Jun 27
• 3 citations
  Gallbladder disease in childhood. Report of four cases including one with "milk of calcium bile".
  Harold N. Bass> ;Clinical Pediatrics. 1970 Apr 1
• 6 citations
  "Bubble Bath'' as an Irritant to the: Urinary Tract of Children
  Harold N. Bass> ;Clinical Pediatrics. 1968 Mar 1
• 6 citations
  Nephrolithiasis In Childhood: Clinical and Etiologic Considerations
  Harold N. Bass, Benjamin Emanuel> ;Clinical Pediatrics. 1966 Feb 1
• Cystic fibrosis presenting with anemia and hypoproteinemia in identical twins.
  Bass, H. N., Miller, A. A.> ;Pediatrics. 1977 Jan
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Journal Articles

• Application of oligonucleotide array CGH to the simultaneous detection of a deletion in the nuclear TK2 gene and mtDNA deletion  
  Zhang S, Li FY, Bass HN, Pursley A, Schmitt ES, Brown BL, Brundage EK, Mardach R, Wong LJ, Mol Genet Metab, 1/1/2010
• Consultations in molecular diagnostics: a pseudo-full mutation identified in fragile X assay reveals a novel base change abolishing an EcoR1 restriction site  
  Liang S, Bass HN, Gao H, Astbury C, Jamehdor M, Qu Y, J Molec Diag, 1/1/2008
• Neonatal asymmetric crying facies: A new look at an old problem  
  Sapin SO, Miller AA, Bass HN, Clin Pediatr, 1/1/2005
• Perinatal screening for congenital malformations and genetic disorders: current status and future directions  
  Bass HN, Beavers Taylor J, Permanente J, 1/1/2002
• Chicago comment: what should be the highest priority in the study of genetics?  
  Bass HN, U of Chicago Medicine on the Midway Spring, 1/1/2000
• Attitudes toward genetic carrier screening for cystic fibrosis among pregnant women: The role of health beliefs and avoidant coping style  
  Fang CY, Dunkel-Schetter C, Tatsugawa ZH, Fox MA, Bass HN, Crandall BF, Grody WW, Women's Health: Research on Gender Behavior Policy, 1/1/1997
• Spontaneous pneumothorax in association with pyridoxine-responsive homocystinuria  
  Bass HN, LaGrave D, Mardach R, Cederbaum SD, Fuster CD, Chetty M, J Inher Metab Dis, 1/1/1997
• Education and testing strategy for large-scale cystic fibrosis carrier screening  
  Tatsugawa ZH, Fox MA, Fang CY, Novak JM, Cantor RM, Bass HN, Dunkel-Schetter C, Crandall BF, Grody WW, J Genet Couns, 1/1/1994
• Michelin tire baby syndrome: Familial constriction bands during infancy and childhood in four generations  
  Bass HN, Caldwell S, Brooks BS, Am J Med Genet, 1/1/1993
• Association of generalized epidermolysis bullosa with positive acetylcholinesterase and markedly elevated maternal serum and amniotic fluid alpha-fetoprotein  
  Bass HN, Miranda C, Oei R, Crandall BF, Prenat Diagn, 1/1/1993
• Miller-Dieker syndrome: Detection of a cryptic translocation by in situ hybridization in a family with multiple affected offspring  
  Alvarado M, Bass HN, Caldwell S, Jamehdor M, Miller AA, Jacob P, Am J Dis Child, 1/1/1993
• Churg-Strauss syndrome in a 12-year-old boy diagnosed by transbronchial biopsy  
  Treitman P, Herskowitz JL, Bass HN, Clin Pediatr, 1/1/1991
• Socioeconomic differences in rates of cesarean section  
  Bass HN, N Engl J Med, 1/1/1990
• Herpesvirus infections of pregnancy  
  Bass HN, N Engl J Med, 1/1/1986
• Evidence from somatic cells for crossing-over in humans  
  Sparkes RS, Sparkes MC, Bass HN, Cytogenet Cell Genet, 1/1/1986
• A family with three independent autosomal translocations associated with 7q327qter syndrome  
  Bass HN, Sparkes RS, Lessner MM, Fox M, Phoenix B, Bernar J, J Med Genet, 1/1/1985
• Infant with partial trisomy 7q in a family with three balanced translocations  
  Bass HN, Sparkes RS, Lessner MM, Fox M, Phoenix B, Clin Res, 1/1/1983
• Marfan-like features and congenital contractural arachnodactyly  
  Bass HN, J Pediatr, 1/1/1982
• Trisomy 18 mosaicism: Clues to the diagnosis  
  Bass HN, Fox M, Wulfsberg E, Sparkes RS, Crandall BF, Clin Genet, 1/1/1982
• Congenital contractural arachnodactyly, keratoconus and probable Marfan syndrome in the same pedigree  
  Bass HN, Sparkes RS, Crandall BF, Marcy SM, J Pediatr, 1/1/1981
• Osteopathia striata syndrome: clinical, genetic and radiologic considerations  
  Bass HN, Weiner JR, Goldman A, Smith LE, Sparkes RS, Crandall BF, Clin Pediatr, 1/1/1980
• Metric merits  
  Bass HN, Hosp Pract, 1/1/1980
• Paroxysmal atrial fibrillation and exposure to smoke  
  Bass HN, Hildreth BF, Lancet, 1/1/1979
• Two balanced in three generations of a pedigree: t(7;10)(q11;q22) and t(14;21)(14qtercen21qter)  
  Bass HN, Sparkes RS, J Med Genet, 1/1/1979
• Health maintenance organizations (HMOs): An American medical opinion  
  Bass HN, Ontario (Canada) Dentist, 1/1/1979
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Books/Book Chapters

• A Comprehensive Approach to Congenital Heart Diseases 
  Chapter: Down Syndrome 
  Page 960 - 969Bass, HN, Chugh REditors: Vijayalakshmi IB, Rao PS, Chugh R.Jaypee Brothers, New Delhi2013
• A comprehensive approach to congenital heart diseases 
  Chapter: Marfan syndrome 
  Page 946 - 959Bass HN, Chugh REditors: Vijayalakshmi IB, Rao PS, Chugh R.Jaypee Brothers, New Delhi2013
• Birth defects compendium 
  Chapter: Aicardi syndrome 
  Page 66 - 68Bass HNEditors: Buyse ML.Blackwell, OxfordEdition 3rd,1990
• Birth defects compendium 
  Chapter: Congenital glaucoma 
  Page 782 - 783Bass HNEditors: Buyse ML.Blackwell, OxfordEdition 3rd,1990
• Birth defects compendium 
  Chapter: Hereditary nephritis and nerve deafness (Alport syndrome) 
  Page 1222 - 1223Bass HNEditors: Buyse ML.Blackwell, OxfordEdition 3rd,1990
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