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Results: 1-25 | 26-41
Results: 1-25/41
PRENATAL-DIAGNOSIS FOR SCHMID METAPHYSEAL CHONDRODYSPLASIA IN TWINS
Authors: MILUNSKY J MAHER T LEBO R MILUNSKY A
Citation: J. Milunsky et al., PRENATAL-DIAGNOSIS FOR SCHMID METAPHYSEAL CHONDRODYSPLASIA IN TWINS, Fetal diagnosis and therapy, 13(3), 1998, pp. 167-168
CORRELATION BETWEEN WAARDENBURG-SYNDROME PHENOTYPE AND GENOTYPE IN A POPULATION OF INDIVIDUALS WITH IDENTIFIED PAX3 MUTATIONS
Authors: DESTEFANO AL CUPPLES LA ARNOS KS ASHER JH BALDWIN CT BLANTON S CAREY ML DASILVA EO FRIEDMAN TB GREENBERG J LALWANI AK MILUNSKY A NANCE WE PANDYA A RAMESAR RS READ AP TASSABEJHI M WILCOX ER FARRER LA
Citation: Al. Destefano et al., CORRELATION BETWEEN WAARDENBURG-SYNDROME PHENOTYPE AND GENOTYPE IN A POPULATION OF INDIVIDUALS WITH IDENTIFIED PAX3 MUTATIONS, Human genetics, 102(5), 1998, pp. 499-506
EVIDENCE FOR GENETIC-HETEROGENEITY OF THE CARNEY COMPLEX (FAMILIAL ATRIAL-MYXOMA SYNDROMES)
Authors: MILUNSKY J HUANG XL BALDWIN CT FARAH MG MILUNSKY A
Citation: J. Milunsky et al., EVIDENCE FOR GENETIC-HETEROGENEITY OF THE CARNEY COMPLEX (FAMILIAL ATRIAL-MYXOMA SYNDROMES), Cancer genetics and cytogenetics, 106(2), 1998, pp. 173-176
RENAL TUBULAR DYSGENESIS WITH MICROCEPHALY
Authors: MILUNSKY JM GENEST DR MILUNSKY A
Citation: Jm. Milunsky et al., RENAL TUBULAR DYSGENESIS WITH MICROCEPHALY, Pediatric nephrology, 11(4), 1997, pp. 494-496
GENETIC-COUNSELING IN PERINATAL MEDICINE
Authors: MILUNSKY JM MILUNSKY A
Citation: Jm. Milunsky et A. Milunsky, GENETIC-COUNSELING IN PERINATAL MEDICINE, Obstetrics and gynecology clinics of North America, 24(1), 1997, pp. 1
FAMILIAL PARAGANGLIOMAS - LINKAGE TO CHROMOSOME 11Q23 AND CLINICAL IMPLICATIONS
Authors: MILUNSKY J DESTEFANO AL HUANG XL BALDWIN CT MICHELS VV JAKO G MILUNSKY A
Citation: J. Milunsky et al., FAMILIAL PARAGANGLIOMAS - LINKAGE TO CHROMOSOME 11Q23 AND CLINICAL IMPLICATIONS, American journal of medical genetics, 72(1), 1997, pp. 66-70
EVIDENCE FOR GENETIC-HETEROGENEITY OF THE CARNEY COMPLEX (FAMILIAL ATRIAL-MYXOMA SYNDROMES)
Authors: MILUNSKY J HUANG XL BALDWIN C FARAH MG MILUNSKY A
Citation: J. Milunsky et al., EVIDENCE FOR GENETIC-HETEROGENEITY OF THE CARNEY COMPLEX (FAMILIAL ATRIAL-MYXOMA SYNDROMES), American journal of human genetics, 61(4), 1997, pp. 406-406
FAMILIAL MOSAICISM FOR SMALL SUPERNUMERARY CHROMOSOMES
Authors: WYANDT HE HUANG XL MILUNSKY J MILUNSKY A
Citation: He. Wyandt et al., FAMILIAL MOSAICISM FOR SMALL SUPERNUMERARY CHROMOSOMES, American journal of human genetics, 61(4), 1997, pp. 2199-2199
EVALUATION OF SATELLITED Y-CHROMOSOME (YQS) DETECTED DURING PRENATAL-DIAGNOSIS
Authors: HADDAD BR HUANG YF WYANDT H MILUNSKY A
Citation: Br. Haddad et al., EVALUATION OF SATELLITED Y-CHROMOSOME (YQS) DETECTED DURING PRENATAL-DIAGNOSIS, Acta obstetricia et gynecologica Scandinavica, 76(3), 1997, pp. 281-283
A NOVEL MUTATION IN THE MITF GENE CAUSES WAARDENBURG-SYNDROME TYPE-2
Authors: LAUTENSCHLAGER NT MILUNSKY A DESTEFANO A FARRER L BALDWIN CT
Citation: Nt. Lautenschlager et al., A NOVEL MUTATION IN THE MITF GENE CAUSES WAARDENBURG-SYNDROME TYPE-2, GENET A-BIO, 13(2), 1996, pp. 43-44
MATERNAL SERUM TRIPLE ANALYTE SCREENING AND ADVERSE PREGNANCY OUTCOME
Authors: MILUNSKY A NEBIOLO L
Citation: A. Milunsky et L. Nebiolo, MATERNAL SERUM TRIPLE ANALYTE SCREENING AND ADVERSE PREGNANCY OUTCOME, Fetal diagnosis and therapy, 11(4), 1996, pp. 249-253
FAMILIAL SUPERNUMERARY CHROMOSOME AND MALIGNANCY
Authors: MILUNSKY JM WYANDT HE MILUNSKY A
Citation: Jm. Milunsky et al., FAMILIAL SUPERNUMERARY CHROMOSOME AND MALIGNANCY, Cancer genetics and cytogenetics, 89(2), 1996, pp. 170-172
TRISOMY 15 MOSAICISM AND UNIPARENTAL DISOMY (UPD) IN A LIVEBORN INFANT
Authors: MILUNSKY JM WYANDT HE HUANG XL KANG XZ ELIAS ER MILUNSKY A
Citation: Jm. Milunsky et al., TRISOMY 15 MOSAICISM AND UNIPARENTAL DISOMY (UPD) IN A LIVEBORN INFANT, American journal of medical genetics, 61(3), 1996, pp. 269-273
CONGENITAL-DEFECTS, FOLIC-ACID, AND HOMOEOBOX GENES
Authors: MILUNSKY A
Citation: A. Milunsky, CONGENITAL-DEFECTS, FOLIC-ACID, AND HOMOEOBOX GENES, Lancet, 348(9025), 1996, pp. 419-420
CHROMOSOMAL TRANSLOCATIONS IN SECONDARY ACUTE MYELOID-LEUKEMIA
Authors: ROWLEY JD VIGNON C GOLLIN SM ROSENBERG CL WYANDT HE MILUNSKY A
Citation: Jd. Rowley et al., CHROMOSOMAL TRANSLOCATIONS IN SECONDARY ACUTE MYELOID-LEUKEMIA, The New England journal of medicine, 334(9), 1996, pp. 601-603
TERATOGENICITY OF HIGH VITAMIN-A INTAKE - REPLY
Authors: ROTHMAN KJ MOORE LL SINGER MR MILUNSKY A
Citation: Kj. Rothman et al., TERATOGENICITY OF HIGH VITAMIN-A INTAKE - REPLY, The New England journal of medicine, 334(18), 1996, pp. 1197-1197
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
PULMONARY-FUNCTION AND CLINICAL OBSERVATIONS IN MEN WITH CONGENITAL BILATERAL ABSENCE OF THE VAS-DEFERENS
Authors: COLIN AA SAWYER SM MICKLE JE OATES RD MILUNSKY A AMOS JA
Citation: Aa. Colin et al., PULMONARY-FUNCTION AND CLINICAL OBSERVATIONS IN MEN WITH CONGENITAL BILATERAL ABSENCE OF THE VAS-DEFERENS, Chest, 110(2), 1996, pp. 440-445
CASE-REPORT - CYSTIC-FIBROSIS AND EMBRYONAL CARCINOMA OF THE TESTIS
Authors: MILUNSKY JM MILUNSKY A
Citation: Jm. Milunsky et A. Milunsky, CASE-REPORT - CYSTIC-FIBROSIS AND EMBRYONAL CARCINOMA OF THE TESTIS, The American journal of the medical sciences, 311(4), 1996, pp. 191-192
CONGENITAL UNILATERAL ABSENCE OF THE VAS-DEFERENS - A HETEROGENEOUS DISORDER WITH 2 DISTINCT SUBPOPULATIONS BASED UPON ETIOLOGY AND MUTATIONAL STATUS OF THE CYSTIC-FIBROSIS GENE
Authors: MICKLE J MILUNSKY A AMOS JA OATES RD
Citation: J. Mickle et al., CONGENITAL UNILATERAL ABSENCE OF THE VAS-DEFERENS - A HETEROGENEOUS DISORDER WITH 2 DISTINCT SUBPOPULATIONS BASED UPON ETIOLOGY AND MUTATIONAL STATUS OF THE CYSTIC-FIBROSIS GENE, Human reproduction, 10(7), 1995, pp. 1728-1735
MUTATIONS IN PAX3 THAT CAUSE WAARDENBURG SYNDROME TYPE-I - 10 NEW MUTATIONS AND REVIEW OF THE LITERATURE
Authors: BALDWIN CT HOTH CF MACINA RA MILUNSKY A
Citation: Ct. Baldwin et al., MUTATIONS IN PAX3 THAT CAUSE WAARDENBURG SYNDROME TYPE-I - 10 NEW MUTATIONS AND REVIEW OF THE LITERATURE, American journal of medical genetics, 58(2), 1995, pp. 115-122
TERATOGENICITY OF HIGH VITAMIN-A INTAKE
Authors: ROTHMAN KJ MOORE LL SINGER MR NGUYEN USDT MANNINO S MILUNSKY A
Citation: Kj. Rothman et al., TERATOGENICITY OF HIGH VITAMIN-A INTAKE, The New England journal of medicine, 333(21), 1995, pp. 1369-1373
CHROMOSOME 13Q DELETION WITH WAARDENBURG SYNDROME - FURTHER EVIDENCE FOR A GENE INVOLVED IN NEURAL CREST FUNCTION ON 13Q
Authors: VANCAMP G VANTHIENEN MN HANDIG I VANROY B RAO VS MILUNSKY A READ AP BALDWIN CT FARRER LA BONDUELLE M STANDAERT L MEIRE F WILLEMS PJ
Citation: G. Vancamp et al., CHROMOSOME 13Q DELETION WITH WAARDENBURG SYNDROME - FURTHER EVIDENCE FOR A GENE INVOLVED IN NEURAL CREST FUNCTION ON 13Q, Journal of Medical Genetics, 32(7), 1995, pp. 531-536
CYTOGENETIC AND MOLECULAR CYTOGENETIC STUDIES OF A CASE OF INTERSTITIAL DELETION OF PROXIMAL 15Q
Authors: TONK V WYANDT HE OSELLA P SKARE J WU BL HADDAD B MILUNSKY A
Citation: V. Tonk et al., CYTOGENETIC AND MOLECULAR CYTOGENETIC STUDIES OF A CASE OF INTERSTITIAL DELETION OF PROXIMAL 15Q, Clinical genetics, 48(3), 1995, pp. 151-155
DISCREPANT CYTOGENETIC AND FISH RESULTS IN A 26-YEAR-OLD MALE WITH EARLY T-CELL ALL
Authors: CHINNAPPAN D WYANDT HE RASTOGI A BLANCHARD R MILUNSKY A
Citation: D. Chinnappan et al., DISCREPANT CYTOGENETIC AND FISH RESULTS IN A 26-YEAR-OLD MALE WITH EARLY T-CELL ALL, American journal of human genetics, 57(4), 1995, pp. 326-326
Risultati: 1-25 | 26-41