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Results:
1-22
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Results: 22
Authors:
WHEELER PG
MEDINA S
DUSICK A
BULL MJ
ANDREOLI SP
EDWARDSBROWN M
WEAVER DD
Citation: Pg. Wheeler et al., LIVEDO-RETICULARIS, DEVELOPMENTAL DELAY AND STROKE-LIKE EPISODE IN A 7-YEAR-OLD MALE, Clinical dysmorphology, 7(1), 1998, pp. 69-74
Authors:
PROUD VK
BRADDOCK SR
COOK L
WEAVER DD
Citation: Vk. Proud et al., WEAVER-SYNDROME - AUTOSOMAL-DOMINANT INHERITANCE OF THE DISORDER, American journal of medical genetics, 79(4), 1998, pp. 305-310
Authors:
KHOSRAVI M
WEAVER DD
BULL MJ
LACHMAN R
RIMOIN DL
Citation: M. Khosravi et al., LETHAL SYNDROME OF SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL-NERVOUS-SYSTEM DEGENERATION, American journal of medical genetics, 77(1), 1998, pp. 63-71
Authors:
PEET J
WEAVER DD
VANCE GH
Citation: J. Peet et al., 49,XXXXY - A DISTINCT PHENOTYPE - 3 NEW CASES AND REVIEW, Journal of Medical Genetics, 35(5), 1998, pp. 420-424
Authors:
WHEELER PG
WEAVER DD
OBEIME MO
VANCE GH
BULL MJ
ESCOBAR LF
Citation: Pg. Wheeler et al., URORECTAL SEPTUM MALFORMATION SEQUENCE - REPORT OF 13 ADDITIONAL CASES AND REVIEW OF THE LITERATURE, American journal of medical genetics, 73(4), 1997, pp. 456-462
Authors:
ZHANG AW
WEAVER DD
PALMER CG
Citation: Aw. Zhang et al., MOLECULAR CYTOGENETIC IDENTIFICATION OF 4 X-CHROMOSOME DUPLICATIONS, American journal of medical genetics, 68(1), 1997, pp. 29-38
Authors:
VANMETER TD
WEAVER DD
Citation: Td. Vanmeter et Dd. Weaver, OCULO-AURICULO-VERTEBRAL SPECTRUM AND THE CHARGE ASSOCIATION - CLINICAL-EVIDENCE FOR A COMMON PATHOGENETIC MECHANISM, Clinical dysmorphology, 5(3), 1996, pp. 187-196
Authors:
PALMER CG
BLOUIN JL
BULL MJ
BREITFELD P
VANCE GH
VANMETER T
WEAVER DD
HEEREMA NA
COLBERN SG
KORENBERG JR
ANTONARAKIS SE
CHEN X
Citation: Cg. Palmer et al., CYTOGENETIC AND MOLECULAR ANALYSIS OF A RING (21) IN A PATIENT WITH PARTIAL TRISOMY-21 AND MEGAKARYOCYTIC LEUKEMIA, American journal of medical genetics, 57(4), 1995, pp. 527-536
Authors:
WHEELER PG
WEAVER DD
PALMER CG
Citation: Pg. Wheeler et al., FAMILIAL TRANSLOCATION RESULTING IN WOLF-HIRSCHHORN-SYNDROME IN 2 RELATED UNBALANCED INDIVIDUALS - CLINICAL-EVALUATION OF A 39-YEAR-OLD MANWITH WOLF-HIRSCHHORN-SYNDROME, American journal of medical genetics, 55(4), 1995, pp. 462-465
Authors:
MEWAR R
HARRISON W
WEAVER DD
PALMER C
DAVEE MA
OVERHAUSER J
Citation: R. Mewar et al., MOLECULAR CYTOGENETIC DETERMINATION OF A DELETION DUPLICATION OF 1Q THAT RESULTS IN A TRISOMY-18 SYNDROME-LIKE PHENOTYPE/, American journal of medical genetics, 52(2), 1994, pp. 178-183
Authors:
MCCOOL M
WEAVER DD
Citation: M. Mccool et Dd. Weaver, BRANCHIOOCULOFACIAL SYNDROME - BROADENING THE SPECTRUM, American journal of medical genetics, 49(4), 1994, pp. 414-421
Authors:
WHEELER PG
WEAVER DD
DOBYNS WB
Citation: Pg. Wheeler et al., BENIGN HEREDITARY CHOREA, Pediatric neurology, 9(5), 1993, pp. 337-340
Authors:
MOORE LA
MOORE CA
SMITH JA
WEAVER DD
Citation: La. Moore et al., ASYMMETRIC AND SYMMETRICAL LONG-BONE BOWING IN 2 SIBS - AN APPARENTLYNEW BONE DYSPLASIA, American journal of medical genetics, 47(7), 1993, pp. 1072-1077
Authors:
VANMETER TD
WEAVER DD
Citation: Td. Vanmeter et Dd. Weaver, OCULO-AURICULO-VERTEBRAL SPECTRUM VS CHARGE ASSOCIATION - ARE THEY TRULY SEPARATE CONDITIONS, American journal of human genetics, 53(3), 1993, pp. 516-516
Authors:
HARRISON W
MEWAR R
SELL L
WEAVER DD
PALMER C
DAVEE M
OVERHAUSER J
Citation: W. Harrison et al., MOLECULAR CYTOGENETIC ANALYSIS OF A DELETION, DUPLICATION CHROMOSOME-1 IN AN INFANT WITH TRISOMY-18 PHENOTYPE, American journal of human genetics, 53(3), 1993, pp. 558-558
Authors:
HOBART HH
ZHANG A
WEAVER DD
VANCE GH
PALMER CG
Citation: Hh. Hobart et al., FREQUENT OCCURRENCE OF DUPLICATIONS AMONG DE-NOVO CHROMOSOME REARRANGEMENTS, American journal of human genetics, 53(3), 1993, pp. 560-560
Authors:
WHEELER PG
WEAVER DD
PALMER CG
Citation: Pg. Wheeler et al., A 4-GENERATION TRANSLOCATION RESULTING IN WOLF-HIRSCHHORN SYNDROME INUNBALANCED INDIVIDUALS - CLINICAL-EVALUATION OF A 39-YEAR-OLD MALE WITH WOLF-HIRSCHHORN SYNDROME, American journal of human genetics, 53(3), 1993, pp. 625-625
Authors:
TORRES W
SAHOTA A
BOYADJIEV S
VANCE GH
WEAVER DD
Citation: W. Torres et al., FRAGILE-X FULL MUTATION IN 2 CLINICALLY UNAFFECTED BROTHERS, American journal of human genetics, 53(3), 1993, pp. 1241-1241
Authors:
KHOSRAVI M
WEAVER DD
Citation: M. Khosravi et Dd. Weaver, EHLERS-DANLOS SYNDROME TYPE-IX (OCCIPITAL HORN SYNDROME) - REPORT OF AN ADDITIONAL CASE, American journal of human genetics, 53(3), 1993, pp. 1548-1548
Authors:
WEAVER DD
HOUSTON L
Citation: Dd. Weaver et L. Houston, DYSBLASTOGENESIS - THE FORMATION OF MALFORMATIONS DURING THE 1ST 4 WEEKS OF DEVELOPMENT, American journal of human genetics, 53(3), 1993, pp. 1604-1604
Authors:
WEAVER DD
BAKER D
THEOBALD M
COHEN F
KING RA
KRUEGER S
LAXOVA R
LUBINSKY MS
Citation: Dd. Weaver et al., MINIMUM GUIDELINES FOR THE DELIVERY OF CLINICAL GENETICS SERVICES, American journal of human genetics, 53(1), 1993, pp. 287-289
Authors:
VANMETER TD
WEAVER DD
Citation: Td. Vanmeter et Dd. Weaver, CONCERNS ABOUT THE GENETICS OF PREECLAMPSIA, American journal of human genetics, 52(5), 1993, pp. 1012-1013
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1-22
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