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1. Cunniff, C; Frias, JL; Kaye, C; Moeschler, JB; Panny, SR; Trotter, TL
   Maternal phenylketonuria
   PEDIATRICS
   
   C. Cunniff et al., "Maternal phenylketonuria", PEDIATRICS, 107(2), 2001, pp. 427-428
2. Cunniff, C; Frias, JL; Kaye, C; Moeschler, JB; Panny, SR; Trotter, TL
   Health supervision for children with Down syndrome
   PEDIATRICS
   
   C. Cunniff et al., "Health supervision for children with Down syndrome", PEDIATRICS, 107(2), 2001, pp. 442-449
3. Cunniff, C; Frias, JL; Kaye, C; Moeschler, JB; Panny, SR; Trotter, TL; Hanson, JW; Williams, J; Moore, CA; Lloyd-Puryear, M; de la Cruz, F; Cho, S; Desposito, F; Hoyme, HE; Hall, L
   Molecular genetic testing in pediatric practice: A subject review
   PEDIATRICS
   
   C. Cunniff et al., "Molecular genetic testing in pediatric practice: A subject review", PEDIATRICS, 106(6), 2000, pp. 1494-1497
4. Frias, J; Levine, LS; Oberfield, SE; Pang, S; Silverstein, J; Schwartz, RP; Hansen, IL; Kaufman, F; Varma, SK; Oberfield, SE; Silverstein, J; Levitsky, L; Suriano, MJ; Poulin, L; Cunniff, C; Frias, JL; Kaye, C; Moeschler, JB; Panny, SR; Trotter, TL; de la Cruz, F; Hanson, JW; Lloyd-Puryear, M; Moore, CA; Williams, J; Hoyme, HE; Hall, L
   Technical report: Congenital adrenal hyperplasia
   PEDIATRICS
   
   J. Frias et al., "Technical report: Congenital adrenal hyperplasia", PEDIATRICS, 106(6), 2000, pp. 1511-1518
5. Mohandas, TK; Park, JP; Spellman, RA; Filiano, JJ; Mamourian, AC; Hawk, AB; Belloni, DR; Noll, WW; Moeschler, JB
   Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay
   AMERICAN JOURNAL OF MEDICAL GENETICS
   
   T.K. Mohandas et al., "Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay", AM J MED G, 82(4), 1999, pp. 294-300
6. PARK JP; MOESCHLER JB; HANI VH; HAWK AB; BELLONI DR; NOLL WW; MOHANDAS TK
   MATERNAL DISOMY AND PRADER-WILLI-SYNDROME CONSISTENT WITH GAMETE COMPLEMENTATION IN A CASE OF FAMILIAL TRANSLOCATION (3-15) (P25-Q11.2)
   American journal of medical genetics
   
   J.P. Park et al., "MATERNAL DISOMY AND PRADER-WILLI-SYNDROME CONSISTENT WITH GAMETE COMPLEMENTATION IN A CASE OF FAMILIAL TRANSLOCATION (3-15) (P25-Q11.2)", American journal of medical genetics, 78(2), 1998, pp. 134-139
7. PARK JP; MOESCHLER JB; DAVIES WS; PATEL PI; MOHANDAS TK
   SMITH-MAGENIS-SYNDROME RESULTING FROM A DE-NOVO DIRECT INSERTION OF PROXIMAL 17Q INTO 17P11.2
   American journal of medical genetics
   
   J.P. Park et al., "SMITH-MAGENIS-SYNDROME RESULTING FROM A DE-NOVO DIRECT INSERTION OF PROXIMAL 17Q INTO 17P11.2", American journal of medical genetics, 77(1), 1998, pp. 23-27
8. PARK JP; MOESCHLER JB
   ISOCHROMOSOME 18Q REVISITED
   Prenatal diagnosis
   
   J.P. Park e J.B. Moeschler, "ISOCHROMOSOME 18Q REVISITED", Prenatal diagnosis, 17(6), 1997, pp. 589-590
9. BUTLER MG; HEDGES LK; ROGAN PK; SEIP JR; CASSIDY SB; MOESCHLER JB
   KLINEFELTER-SYNDROME AND TRISOMY-X-SYNDROME IN PATIENTS WITH PRADER-WILLI-SYNDROME AND UNIPARENTAL MATERNAL DISOMY OF CHROMOSOME-15 - A COINCIDENCE
   American journal of medical genetics
   
   M.G. Butler et al., "KLINEFELTER-SYNDROME AND TRISOMY-X-SYNDROME IN PATIENTS WITH PRADER-WILLI-SYNDROME AND UNIPARENTAL MATERNAL DISOMY OF CHROMOSOME-15 - A COINCIDENCE", American journal of medical genetics, 72(1), 1997, pp. 111-114
10. WENG EY; MOESCHLER JB; GRAHAM JM
    LONGITUDINAL OBSERVATIONS ON 15 CHILDREN WITH WIEDEMANN-BECKWITH SYNDROME
    American journal of medical genetics
    
    E.Y. Weng et al., "LONGITUDINAL OBSERVATIONS ON 15 CHILDREN WITH WIEDEMANN-BECKWITH SYNDROME", American journal of medical genetics, 56(4), 1995, pp. 366-373
11. MOESCHLER JB; FILIANO JJ; HANI V; RAWNSLEY E
    MOTHER AND DAUGHTER DEMONSTRATING FEATURES OF BOTH ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT-PALATE (MIM-NUMBER-106250) AND HAY-WELLS SYNDROME (MIM-NUMBER-106260)
    American journal of human genetics
    
    J.B. Moeschler et al., "MOTHER AND DAUGHTER DEMONSTRATING FEATURES OF BOTH ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT-PALATE (MIM-NUMBER-106250) AND HAY-WELLS SYNDROME (MIM-NUMBER-106260)", American journal of human genetics, 57(4), 1995, pp. 95-95
12. BUTLER MG; HEDGES LK; MOESCHLER JB
    12-YEAR-OLD FEMALE WITH BOTH PRADER-WILLI AND TRISOMY-X SYNDROMES
    American journal of human genetics
    
    M.G. Butler et al., "12-YEAR-OLD FEMALE WITH BOTH PRADER-WILLI AND TRISOMY-X SYNDROMES", American journal of human genetics, 57(4), 1995, pp. 609-609
13. HANI VH; PARK J; ALLEN EF; MOESCHLER JB
    PARACENTRIC INVERSION OF CHROMOSOME-18 WITH DUPLICATION OF THE INVERTED MATERIAL IN A CHILD DUE TO A MATERNAL PARACENTRIC INVERSION OF 18Q
    American journal of human genetics
    
    V.H. Hani et al., "PARACENTRIC INVERSION OF CHROMOSOME-18 WITH DUPLICATION OF THE INVERTED MATERIAL IN A CHILD DUE TO A MATERNAL PARACENTRIC INVERSION OF 18Q", American journal of human genetics, 57(4), 1995, pp. 642-642
14. MOESCHLER JB; GRAHAM JM
    MILD BRACHMANN-DELANGE SYNDROME - PHENOTYPIC AND DEVELOPMENTAL CHARACTERISTICS OF MILDLY AFFECTED INDIVIDUALS
    American journal of medical genetics
    
    J.B. Moeschler e J.M. Graham, "MILD BRACHMANN-DELANGE SYNDROME - PHENOTYPIC AND DEVELOPMENTAL CHARACTERISTICS OF MILDLY AFFECTED INDIVIDUALS", American journal of medical genetics, 47(7), 1993, pp. 969-976
15. BRADDOCK SR; LACHMAN RS; STOPPENHAGEN CC; CAREY JC; IRELAND M; MOESCHLER JB; CUNNIFF C; GRAHAM JM
    RADIOLOGICAL FEATURES IN BRACHMANN-DELANGE SYNDROME
    American journal of medical genetics
    
    S.R. Braddock et al., "RADIOLOGICAL FEATURES IN BRACHMANN-DELANGE SYNDROME", American journal of medical genetics, 47(7), 1993, pp. 1006-1013
16. PARK JP; MCDERMET MK; MOESCHLER JB; WURSTERHILL DH
    A CASE OF DE-NOVO TRANSLOCATION 7-10 AND THE DUPLICATION 7P, DELETION10P PHENOTYPE
    Annales de genetique
    
    J.P. Park et al., "A CASE OF DE-NOVO TRANSLOCATION 7-10 AND THE DUPLICATION 7P, DELETION10P PHENOTYPE", Annales de genetique, 36(4), 1993, pp. 217-220