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Results:
1-12
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Results: 12
Authors:
GELB BD
WILLNER JP
DUNN TM
KARDON NB
VERLOES A
PONCIN J
DESNICK RJ
Citation: Bd. Gelb et al., PATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-1 REVEALED BY MOLECULAR ANALYSIS OF A PATIENT WITH PYCNODYSOSTOSIS, American journal of human genetics, 62(4), 1998, pp. 848-854
Authors:
COTTER PD
BABU A
WILLNER JP
DESNICK RJ
Citation: Pd. Cotter et al., PRENATAL-DIAGNOSIS AND OUTCOME OF MOSAICISM FOR A DE-NOVO UNBALANCED TRANSLOCATION IDENTIFIED IN AMNIOCYTES, Prenatal diagnosis, 18(8), 1998, pp. 857-861
Authors:
WILLNER JP
Citation: Jp. Willner, REPRODUCTIVE GENETICS AND TODAYS PATIENT OPTIONS - PRENATAL-DIAGNOSIS, The Mount Sinai journal of medicine, 65(3), 1998, pp. 173-177
Authors:
ASHTONPROLLA P
GERSHIN IF
BABU A
NEU RL
ZINBERG RE
WILLNER JP
DESNICK RJ
COTTER PD
Citation: P. Ashtonprolla et al., PRENATAL-DIAGNOSIS OF A FAMILIAL INTERCHROMOSOMAL INSERTION OF Y-CHROMOSOME HETEROCHROMATIN, American journal of medical genetics, 73(4), 1997, pp. 470-473
Authors:
COTTER PD
MCCURDY LD
GERSHIN IF
BABU A
WILLNER JP
DESNICK RJ
Citation: Pd. Cotter et al., PRENATAL DETECTION AND MOLECULAR CHARACTERIZATION OF A DE-NOVO DUPLICATION OF THE DISTAL LONG ARM OF CHROMOSOME-19, American journal of medical genetics, 71(3), 1997, pp. 325-328
Authors:
COTTER PD
KAFFE S
MCCURDY LD
JHAVERI M
WILLNER JP
HIRSCHHORN K
Citation: Pd. Cotter et al., PATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-14 - A CASE-REPORT AND REVIEW, American journal of medical genetics, 70(1), 1997, pp. 74-79
Authors:
MACGOWAN DJL
SIVAK M
WILLNER JP
SINGER M
DESNICK RJ
Citation: Djl. Macgowan et al., A UNIQUE CLINICAL-PATTERN OF WEAKNESS AND RADIOLOGIC ABNORMALITIES INPATIENTS WITH LATE-ONSET TAY-SACHS-DISEASE, Neurology, 48(3), 1997, pp. 4024-4024
Authors:
MANEA SR
GERSHIN IF
BABU A
WILLNER JP
DESNICK RJ
COTTER PD
Citation: Sr. Manea et al., MOSAICISM FOR A SMALL SUPERNUMERARY RING X-CHROMOSOME IN A DYSMORPHIC, GROWTH-RETARDED MALE - MOS47,XXY 48,XXY,+R(X)/, Clinical genetics, 52(6), 1997, pp. 432-435
Authors:
COTTER PD
BABU A
MCCURDY LD
CAGGANA M
WILLNER JP
DESNICK RJ
Citation: Pd. Cotter et al., HOMOZYGOSITY FOR PERICENTRIC INVERSIONS OF CHROMOSOME-9 - PRENATAL-DIAGNOSIS OF 2 CASES, Annales de genetique, 40(4), 1997, pp. 222-226
Authors:
GELB BD
WILLNER JP
VERLOES A
HERENS C
DESNICK RJ
Citation: Bd. Gelb et al., MUTATION ANALYSIS OF PYCNODYSOSTOSIS REVEALS UNIPARENTAL DISOMY OF CHROMOSOME-1, American journal of human genetics, 61(4), 1997, pp. 203-203
Authors:
COTTER PD
CAGGANA M
WILLNER JP
BABU A
DESNICK RJ
Citation: Pd. Cotter et al., PRENATAL-DIAGNOSIS OF A FETUS WITH 2 BALANCED DE-NOVO CHROMOSOME REARRANGEMENTS, American journal of medical genetics, 66(2), 1996, pp. 197-199
Authors:
PASTORES GM
SANTORELLI FM
SHANSKE S
GELB BD
FYFE B
WOLFE D
WILLNER JP
Citation: Gm. Pastores et al., LEIGH-SYNDROME AND HYPERTROPHIC CARDIOMYOPATHY IN AN INFANT WITH A MITOCHONDRIAL-DNA POINT MUTATION (T8993G), American journal of medical genetics, 50(3), 1994, pp. 265-271
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