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Results:
1-23
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Results: 23
Authors:
LIN AE
WESTGATE MN
VANDERVELDE ME
LACRO RV
HOLMES LB
Citation: Ae. Lin et al., ADAMS-OLIVER-SYNDROME ASSOCIATED WITH CARDIOVASCULAR MALFORMATIONS, Clinical dysmorphology, 7(4), 1998, pp. 235-241
Authors:
LIN AE
LIPPE B
ROSENFELD RG
Citation: Ae. Lin et al., FURTHER DELINEATION OF AORTIC DILATION, DISSECTION, AND RUPTURE IN PATIENTS WITH TURNER-SYNDROME, Pediatrics (Evanston), 102(1), 1998, pp. 121-129
Authors:
LIN AE
ROSTI L
Citation: Ae. Lin et L. Rosti, TRICUSPID-ATRESIA IN SIBS, Journal of Medical Genetics, 35(12), 1998, pp. 1055-1056
Authors:
BLAKE KD
DAVENPORT SLH
HALL BD
HEFNER MA
PAGON RA
WILLIAMS MS
LIN AE
GRAHAM JM
Citation: Kd. Blake et al., CHARGE ASSOCIATION - AN UPDATE AND REVIEW FOR THE PRIMARY PEDIATRICIAN, Clinical pediatrics, 37(3), 1998, pp. 159-173
Authors:
MENGER H
LIN AE
TORIELLO HV
BERNERT G
SPRANGER JW
Citation: H. Menger et al., VITAMIN-K DEFICIENCY EMBRYOPATHY - A PHENOCOPY OF THE WARFARIN EMBRYOPATHY DUE TO A DISORDER OF EMBRYONIC VITAMIN-K METABOLISM, American journal of medical genetics, 72(2), 1997, pp. 129-134
Authors:
LIN AE
ARDINGER HH
ARDINGER RH
CUNNIFF C
KELLEY RI
Citation: Ae. Lin et al., CARDIOVASCULAR MALFORMATIONS IN SMITH-LEMLI-OPITZ SYNDROME, American journal of medical genetics, 68(3), 1997, pp. 270-278
Authors:
LIN AE
LACRO RV
WESTGATE MN
VANDERVELDE M
HOLMES LB
Citation: Ae. Lin et al., ADAMS-OLIVER-SYNDROME WITH CARDIOVASCULAR MALFORMATIONS OF THE LEFT-HEART, American journal of human genetics, 61(4), 1997, pp. 590-590
Authors:
PIVNICK EK
SHAEFER GB
LIN AE
PARK VM
TOLLEY EA
LAWRENCE MD
HUSON SM
Citation: Ek. Pivnick et al., DELINEATION OF A COMMON FACIAL APPEARANCE IN NEUROFIBROMATOSIS TYPE-1(NF1), American journal of human genetics, 61(4), 1997, pp. 616-616
Authors:
LIN AE
Citation: Ae. Lin, THE VALUE OF AORTIC-VALVE AND AORTIC-ARCH IMAGING IN THE IDENTIFICATION OF GENETIC SYNDROMES, Echocardiography, 13(4), 1996, pp. 447-457
Authors:
ROSTI L
LIN AE
FRIGIOLA A
Citation: L. Rosti et al., NEUROBLASTOMA AND CONGENITAL CARDIOVASCULAR MALFORMATIONS, Pediatrics, 97(2), 1996, pp. 258-261
MOLECULAR CYTOGENETIC CHARACTERIZATION OF THE FIRST FAMILIAL CASE OF PARTIAL 9P DUPLICATION (P22P24)
Authors:
HADDAD BR
LIN AE
WYANDT H
MILUNSKY A
Citation: Br. Haddad et al., MOLECULAR CYTOGENETIC CHARACTERIZATION OF THE FIRST FAMILIAL CASE OF PARTIAL 9P DUPLICATION (P22P24), Journal of Medical Genetics, 33(12), 1996, pp. 1045-1047
Authors:
GONG H
LINN WS
SHAMOO DA
ANDERSON KR
NUGENT CA
CLARK KW
LIN AE
Citation: H. Gong et al., EFFECT OF INHALED SALMETEROL ON SULFUR DIOXIDE-INDUCED BRONCHOCONSTRICTION IN ASTHMATIC SUBJECTS, Chest, 110(5), 1996, pp. 1229-1235
Authors:
SCHWARTZ ML
COX GF
LIN AE
KORSON MS
PEREZATAYDE A
LACRO RV
LIPSHULTZ SE
Citation: Ml. Schwartz et al., CLINICAL APPROACH TO GENETIC CARDIOMYOPATHY IN CHILDREN, Circulation, 94(8), 1996, pp. 2021-2038
Authors:
RAMER JC
LIN AE
DOBYNS WB
WINTER R
AYME S
PALLOTTA R
LADDA RL
Citation: Jc. Ramer et al., PREVIOUSLY APPARENTLY UNDESCRIBED SYNDROME - SHALLOW ORBITS, PTOSIS, COLOBOMA, TRIGONOCEPHALY, GYRAL MALFORMATIONS, AND MENTAL AND GROWTH-RETARDATION, American journal of medical genetics, 57(3), 1995, pp. 403-409
Authors:
LIN AE
GORLIN RJ
LURIE IW
BRUNNER HG
VANDERBURGT I
NAUMCHIK IV
RUMYANTSEVA NV
STENGELRUTKOWSKI S
ROSENBAUM K
MEINECKE P
MULLER D
Citation: Ae. Lin et al., FURTHER DELINEATION OF THE BRANCHIOOCULOFACIAL SYNDROME, American journal of medical genetics, 56(1), 1995, pp. 42-59
Authors:
LIN AE
GORLIN RJ
Citation: Ae. Lin et Rj. Gorlin, UNTITLED, Pediatric pathology, 14(1), 1994, pp. 177-177
Authors:
LIN AE
PEXIEDER T
Citation: Ae. Lin et T. Pexieder, NEED FOR GREATER PRECISION IN REPORTING CARDIOVASCULAR MALFORMATIONS, American journal of medical genetics, 51(1), 1994, pp. 84-85
Authors:
FEINGOLD M
LIN AE
Citation: M. Feingold et Ae. Lin, FAMILIAL BRACHMANN-DELANGE SYNDROME - FURTHER EVIDENCE FOR AUTOSOMAL-DOMINANT INHERITANCE AND REVIEW OF THE LITERATURE, American journal of medical genetics, 47(7), 1993, pp. 1064-1067
Authors:
LIN AE
Citation: Ae. Lin, FURTHER DELINEATION OF THE SIMPSON-GOLABI-BEHMEL (SGB) SYNDROME, American journal of medical genetics, 46(5), 1993, pp. 606-606
Authors:
LIN AE
HARSTER GA
Citation: Ae. Lin et Ga. Harster, ANOTHER CASE OF SPONDYLOCOSTAL DYSPLASIA AND SEVERE ANOMALIES, American journal of medical genetics, 46(4), 1993, pp. 476-477
Authors:
LIN AE
BRADDOCK BE
THAYER B
MILLER WA
Citation: Ae. Lin et al., EDUCATING THE OBSTETRIC COMMUNITY THROUGH A GENETIC NEWSLETTER, American journal of human genetics, 53(6), 1993, pp. 1366-1367
Authors:
LIN AE
FEINGOLD M
SIEGEL B
Citation: Ae. Lin et al., OUT, OUT DAMN SPOT, OR THE DEMISE OF THE MONGOLIAN SPOT, American journal of diseases of children [1960], 147(7), 1993, pp. 714-714
Authors:
FEINGOLD M
FRIAS J
LIN AE
SCHAEFER GB
HORWITZ M
Citation: M. Feingold et al., TELEDIAGNOSTIC CONFERENCING, American journal of diseases of children [1960], 147(11), 1993, pp. 1196-1196
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