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Results:
1-21
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Results: 21
Authors:
BECKER JL
PAPENHAUSEN PR
WIDEN RH
Citation: Jl. Becker et al., CYTOGENETIC, MORPHOLOGIC ACID ONCOGENE ANALYSIS OF A CELL-LINE DERIVED FROM A HETEROLOGOUS MIXED MULLERIAN TUMOR OF THE OVARY, In vitro cellular & developmental biology. Animal, 33(5), 1997, pp. 325-331
Authors:
REDDY PP
PAPENHAUSEN PR
SUH YM
RIDDICK LM
CALVANO CJ
MANDELL J
Citation: Pp. Reddy et al., XX-SEX REVERSAL - MOLECULAR ANALYSIS OF THE SRY ZFY-REGIONS/, The Journal of urology, 158(3), 1997, pp. 1305-1307
Authors:
PAPENHAUSEN PR
TEPPERBERG JH
MOWREY PN
TURK K
GADI IK
Citation: Pr. Papenhausen et al., MLL GENE AMPLIFICATION IN MDS AML, American journal of human genetics, 61(4), 1997, pp. 420-420
Authors:
MOWREY PN
GADI IK
TEPPERBERG JH
ALLAHHAM M
KUKOLICH MK
PAPENHAUSEN PR
Citation: Pn. Mowrey et al., UNUSUAL FAMILIAL ADD(15) CHROMOSOME CONTAINS NECESSARY Y-GENES FOR FERTILITY, American journal of human genetics, 61(4), 1997, pp. 767-767
Authors:
TEPPERBERG JH
WILLIFORD B
KAMMORGAN LNW
BINNIE CG
EISENBERG M
MOWREY PN
GADI IK
MENGDEN G
KHODR G
PAPENHAUSEN PR
Citation: Jh. Tepperberg et al., PRADER-WILLI-SYNDROME RT-PCR ANALYSIS USING CULTURED-CELLS FIXED FOR CYTOGENETIC STUDIES, American journal of human genetics, 61(4), 1997, pp. 2383-2383
Authors:
PAPENHAUSEN PR
MUELLER OT
SUTCLIFFE M
DIAMOND TM
KOUSSEFF BG
JOHNSON VP
Citation: Pr. Papenhausen et al., UNIPARENTAL ISODISOMY OF CHROMOSOME-14 IN 2 CASES - AN ABNORMAL CHILDAND A NORMAL ADULT, American journal of medical genetics, 66(1), 1996, pp. 90-90
Authors:
ROGAN PK
SEIP JR
DRISCOLL DJ
PAPENHAUSEN PR
JOHNSON VP
RASKIN S
WOODWARD AL
BUTLER MG
Citation: Pk. Rogan et al., DISTINCT 15Q GENOTYPES IN RUSSELL-SILVER AND RING-15 SYNDROMES, American journal of medical genetics, 62(1), 1996, pp. 10-15
Authors:
REDDY PP
PAPENHAUSEN PR
LUCE M
REDDICK LM
CALVANO CJ
MANDELL J
Citation: Pp. Reddy et al., XX SEX REVERSAL - A MOLECULAR ANALYSIS OF THE SRY ZEY REGIONS/, Pediatrics, 98(3), 1996, pp. 79-79
Authors:
JOSEPH M
CANTU ES
PAI GS
WILLI SM
PAPENHAUSEN PR
WEISS L
Citation: M. Joseph et al., XP PSEUDOAUTOSOMAL GENE HAPLOINSUFFICIENCY AND LINEAR GROWTH DEFICIENCY IN 3 GIRLS WITH CHROMOSOME XP22-YQ11 TRANSLOCATION, Journal of Medical Genetics, 33(11), 1996, pp. 906-911
Authors:
AGALIOTIS DP
PAPENHAUSEN PR
MOSCINSKI LC
ELFENBEIN GJ
Citation: Dp. Agaliotis et al., CASE-REPORT OF SPONTANEOUS REMISSION OF CYTOGENETIC RELAPSE OF CHRONIC MYELOGENOUS-LEUKEMIA SUGGESTIVE OF PROGRESSION TO BLAST CRISIS AFTERALLOGENEIC BONE-MARROW TRANSPLANTATION, Annals of hematology, 70(1), 1995, pp. 37-41
Authors:
PAPENHAUSEN PR
MUELLER OT
JOHNSON VP
SUTCLIFFE M
DIAMOND TM
KOUSSEFF BG
Citation: Pr. Papenhausen et al., UNIPARENTAL ISODISOMY OF CHROMOSOME-14 IN 2 CASES - AN ABNORMAL CHILDAND A NORMAL ADULT, American journal of medical genetics, 59(3), 1995, pp. 271-275
Authors:
LEVINE JG
ROSSI MR
GADI IG
PAPENHAUSEN PR
Citation: Jg. Levine et al., DICENTRIC, TETRACENTRIC, AND OCTOCENTRIC RING CHROMOSOME-15 IN AML-M(6), American journal of human genetics, 57(4), 1995, pp. 373-373
Authors:
HUANG B
CROLLA JA
PAPENHAUSEN PR
LEDBETTER DH
Citation: B. Huang et al., IDENTIFICATION OF 2 CLASSES OF BREAKPOINTS IN SMALL INV DUP(15) CHROMOSOMES BY CYTOGENETIC AND MOLECULAR STUDIES, American journal of human genetics, 57(4), 1995, pp. 651-651
Authors:
PAPENHAUSEN PR
LUCE M
GADI IK
TEPPERBERG JH
ANDERSON SA
Citation: Pr. Papenhausen et al., MOLECULAR ANALYSIS OF SRY ZFY IN CASES OF PHENOTYPE GENOTYPE SEX DISCORDANCE/, American journal of human genetics, 57(4), 1995, pp. 681-681
Authors:
TEPPERBERG JH
GADI IK
ANDERSON SM
ROSSI MR
DEJESUS A
PAPENHAUSEN PR
Citation: Jh. Tepperberg et al., MOLECULAR ANALYSIS OF A RARE MOSAIC-RING-21 CHROMOSOME IN A YOUNG GIRL WITH MILD FEATURES OF DOWN-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 721-721
Authors:
BUTLER MG
WOODWARD AL
DRISCOLL DJ
PAPENHAUSEN PR
JOHNSON VP
RASKIN S
ROGAN PK
Citation: Mg. Butler et al., MOLECULAR-GENETIC ANALYSIS OF 15Q-]QTER MARKERS IN PATIENTS WITH RING-15 AND RUSSELL-SILVER-SYNDROMES, Cytogenetics and cell genetics, 67(1), 1994, pp. 15-15
Authors:
SABA HI
NADEEM SQ
MOSCINSKI LC
SPIERS ASD
PAPENHAUSEN PR
Citation: Hi. Saba et al., IDENTIFICATION OF A NEW CYTOGENETIC ABNORMALITY T(3 21) (Q21 Q22) IN PRIMARY MYELODYSPLASTIC SYNDROME, Blood, 82(10), 1993, pp. 10000556-10000556
Authors:
DIAMOND TM
MUELLER OT
SUTCLIFFE M
PAPENHAUSEN PR
TEDESCO TA
KOUSSEFF BG
Citation: Tm. Diamond et al., UNIPARENTAL DISOMY FOR CHROMOSOME-14 - EVIDENCE FOR AN IMPRINTING EFFECT, American journal of human genetics, 53(3), 1993, pp. 541-541
Authors:
BUTLER MG
DRISCOLL DJ
PAPENHAUSEN PR
JOHNSON VP
ROGAN PK
Citation: Mg. Butler et al., ANALYSIS OF 15Q25-]QTER MARKERS IN PATIENTS WITH RING-15 AND RUSSELL-SILVER SYNDROMES, American journal of human genetics, 53(3), 1993, pp. 1135-1135
Authors:
SUTCLIFFE MJ
MUELLER OT
GALLARDO LA
PAPENHAUSEN PR
TEDESCO TA
Citation: Mj. Sutcliffe et al., MATERNAL ISODISOMY 16 IN A NORMAL 46, XX FOLLOWING TRISOMIC CONCEPTION, American journal of human genetics, 53(3), 1993, pp. 1464-1464
Authors:
JERVIS GA
PAPENHAUSEN PR
KOUSSEFF BG
Citation: Ga. Jervis et al., CHROMOSOME PAINT IN THE DETERMINATION OF DE-NOVO TRANSLOCATION, American journal of human genetics, 53(3), 1993, pp. 1577-1577
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1-21
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