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Items: 1 to 50 of 125

1.

Two polymorphs of trans-[3-(3-nitro-phen-yl)oxiran-2-yl](phen-yl)methanone.

Greenberg FH, Nazarenko AY.

Acta Crystallogr E Crystallogr Commun. 2016 Jun 28;72(Pt 7):1054-9. doi: 10.1107/S2056989016010239. eCollection 2016 Jul 1.

2.

Crystal structure of dimethyl 3,4,5,6-tetra-phenyl-cyclo-hexa-3,5-diene-1,2-di-carboxyl-ate.

Greenberg FH, Nazarenko AY.

Acta Crystallogr E Crystallogr Commun. 2016 Jun 14;72(Pt 7):947-50. doi: 10.1107/S2056989016009403. eCollection 2016 Jul 1.

3.

Crystal structure of 1,2-di-benzoyl-ace-naphthyl-ene.

Greenberg FH, Nazarenko AY.

Acta Crystallogr E Crystallogr Commun. 2015 Jun 13;71(Pt 7):o487-8. doi: 10.1107/S2056989015011160. eCollection 2015 Jul 1.

4.

The face of Smith-Magenis syndrome: a subjective and objective study.

Allanson JE, Greenberg F, Smith AC.

J Med Genet. 1999 May;36(5):394-7.

5.

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder.

Grimbacher B, Holland SM, Gallin JI, Greenberg F, Hill SC, Malech HL, Miller JA, O'Connell AC, Puck JM.

N Engl J Med. 1999 Mar 4;340(9):692-702.

6.

Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.

Wu YQ, Sutton VR, Nickerson E, Lupski JR, Potocki L, Korenberg JR, Greenberg F, Tassabehji M, Shaffer LG.

Am J Med Genet. 1998 Jun 16;78(1):82-9.

PMID:
9637430
7.

Sleep disturbance in Smith-Magenis syndrome (del 17 p11.2).

Smith AC, Dykens E, Greenberg F.

Am J Med Genet. 1998 Mar 28;81(2):186-91.

PMID:
9613860
8.

Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2).

Smith AC, Dykens E, Greenberg F.

Am J Med Genet. 1998 Mar 28;81(2):179-85. Review.

PMID:
9613859
9.

Williams syndrome and the brain.

Lenhoff HM, Wang PP, Greenberg F, Bellugi U.

Sci Am. 1997 Dec;277(6):68-73. No abstract available.

PMID:
9388834
10.

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

Shapira SK, McCaskill C, Northrup H, Spikes AS, Elder FF, Sutton VR, Korenberg JR, Greenberg F, Shaffer LG.

Am J Hum Genet. 1997 Sep;61(3):642-50.

11.

The Pointer syndrome: a new syndrome with skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties.

Huq AH, Braverman RM, Greenberg F, Bacino CA, Rimoin DL, Lachman RS, Levin ML.

Am J Med Genet. 1997 Jan 20;68(2):225-30.

PMID:
9028464
12.

Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients.

Trask BJ, Mefford H, van den Engh G, Massa HF, Juyal RC, Potocki L, Finucane B, Abuelo DN, Witt DR, Magenis E, Baldini A, Greenberg F, Lupski JR, Patel PI.

Hum Genet. 1996 Dec;98(6):710-8.

PMID:
8931707
13.

Ophthalmic manifestations of Smith-Magenis syndrome.

Chen RM, Lupski JR, Greenberg F, Lewis RA.

Ophthalmology. 1996 Jul;103(7):1084-91. Review.

PMID:
8684798
14.

Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy.

Roa BB, Greenberg F, Gunaratne P, Sauer CM, Lubinsky MS, Kozma C, Meck JM, Magenis RE, Shaffer LG, Lupski JR.

Hum Genet. 1996 May;97(5):642-9.

PMID:
8655146
15.

Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients.

Juyal RC, Figuera LE, Hauge X, Elsea SH, Lupski JR, Greenberg F, Baldini A, Patel PI.

Am J Hum Genet. 1996 May;58(5):998-1007.

16.

Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)

Greenberg F, Lewis RA, Potocki L, Glaze D, Parke J, Killian J, Murphy MA, Williamson D, Brown F, Dutton R, McCluggage C, Friedman E, Sulek M, Lupski JR.

Am J Med Genet. 1996 Mar 29;62(3):247-54.

PMID:
8882782
17.

A clinical and molecular study of mosaicism for trisomy 17.

Shaffer LG, McCaskill C, Hersh JH, Greenberg F, Lupski JR.

Hum Genet. 1996 Jan;97(1):69-72.

PMID:
8557263
18.

Hispanic origin and neural tube defects in Houston/Harris County, Texas. II. Risk factors.

Canfield MA, Annegers JF, Brender JD, Cooper SP, Greenberg F.

Am J Epidemiol. 1996 Jan 1;143(1):12-24.

PMID:
8533743
19.

Hispanic origin and neural tube defects in Houston/Harris County, Texas. I. Descriptive epidemiology.

Canfield MA, Annegers JF, Brender JD, Cooper SP, Greenberg F.

Am J Epidemiol. 1996 Jan 1;143(1):1-11.

PMID:
8533740
20.

Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.

Elsea SH, Juyal RC, Jiralerspong S, Finucane BM, Pandolfo M, Greenberg F, Baldini A, Stover P, Patel PI.

Am J Hum Genet. 1995 Dec;57(6):1342-50.

21.

Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient.

Juyal RC, Finucane B, Shaffer LG, Lupski JR, Greenberg F, Scott CI, Baldini A, Patel PI.

Am J Med Genet. 1995 Nov 20;59(3):406-7. No abstract available.

PMID:
8599375
22.

Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization.

Juyal RC, Greenberg F, Mengden GA, Lupski JR, Trask BJ, van den Engh G, Lindsay EA, Christy H, Chen KS, Baldini A, et al.

Am J Med Genet. 1995 Sep 11;58(3):286-91.

PMID:
8533833
23.

A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2.

Kobayashi H, Baumbach L, Matise TC, Schiavi A, Greenberg F, Hoffman EP.

Hum Mol Genet. 1995 Jul;4(7):1213-6.

PMID:
8528211
24.

Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter).

Scheuerle A, Zenger-Hain JL, Van Dyke DL, Ledbetter DH, Greenberg F, Shaffer LG.

Am J Med Genet. 1995 May 8;56(4):403-8.

PMID:
7604850
25.

Dysmorphic features in patients with complex glycerol kinase deficiency.

Scheuerle A, Greenberg F, McCabe ER.

J Pediatr. 1995 May;126(5 Pt 1):764-7.

PMID:
7752004
26.

Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.

Nickerson E, Greenberg F, Keating MT, McCaskill C, Shaffer LG.

Am J Hum Genet. 1995 May;56(5):1156-61.

27.

De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterization.

Lindsay EA, Shaffer LG, Carrozzo R, Greenberg F, Baldini A.

Am J Med Genet. 1995 Apr 10;56(3):296-9.

PMID:
7778594
28.

The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients.

Zhao Z, Lee CC, Jiralerspong S, Juyal RC, Lu F, Baldini A, Greenberg F, Caskey CT, Patel PI.

Hum Mol Genet. 1995 Apr;4(4):589-97.

PMID:
7633408
29.

Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region.

Lindsay EA, Greenberg F, Shaffer LG, Shapira SK, Scambler PJ, Baldini A.

Am J Med Genet. 1995 Mar 27;56(2):191-7.

PMID:
7625444
30.

The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2.

Chen KS, Gunaratne PH, Hoheisel JD, Young IG, Miklos GL, Greenberg F, Shaffer LG, Campbell HD, Lupski JR.

Am J Hum Genet. 1995 Jan;56(1):175-82.

31.

Very low maternal serum chorionic gonadotropin levels in association with fetal triploidy.

Schmidt D, Shaffer LG, McCaskill C, Rose E, Greenberg F.

Am J Obstet Gynecol. 1994 Jan;170(1 Pt 1):77-80.

PMID:
7507646
32.

Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18.

Mewar R, Kline AD, Harrison W, Rojas K, Greenberg F, Overhauser J.

Am J Hum Genet. 1993 Dec;53(6):1269-78. Review.

33.

An additional case of pachygyria, joint contractures and facial abnormalities.

Levin ML, Lupski JR, Carpenter RJ Jr, Gerson LP, Greenberg F.

Clin Dysmorphol. 1993 Oct;2(4):365-8. Review.

PMID:
8305968
34.

DiGeorge syndrome: an historical review of clinical and cytogenetic features.

Greenberg F.

J Med Genet. 1993 Oct;30(10):803-6. Review. No abstract available.

35.

Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion.

Zori RT, Lupski JR, Heju Z, Greenberg F, Killian JM, Gray BA, Driscoll DJ, Patel PI, Zackowski JL.

Am J Med Genet. 1993 Sep 15;47(4):504-11.

PMID:
8256814
36.

Williams syndrome: autosomal dominant inheritance.

Morris CA, Thomas IT, Greenberg F.

Am J Med Genet. 1993 Sep 15;47(4):478-81.

PMID:
8256809
37.

Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation.

Shaffer LG, Hecht JT, Ledbetter DH, Greenberg F.

Am J Med Genet. 1993 Mar 1;45(5):581-3.

PMID:
8456828
38.

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

Mutirangura A, Greenberg F, Butler MG, Malcolm S, Nicholls RD, Chakravarti A, Ledbetter DH.

Hum Mol Genet. 1993 Feb;2(2):143-51.

39.

Prader-Willi syndrome: consensus diagnostic criteria.

Holm VA, Cassidy SB, Butler MG, Hanchett JM, Greenswag LR, Whitman BY, Greenberg F.

Pediatrics. 1993 Feb;91(2):398-402.

40.

Marketing Supported EmploymentMainstream Jobs for Persons with the Most Severe Disabilities.

Greenberg FS.

Work. 1993;3(2):34-8. doi: 10.3233/WOR-1993-3208. No abstract available.

PMID:
24442023
41.

Gene dosage as a mechanism for a common autosomal dominant peripheral neuropathy: Charcot-Marie-Tooth disease type 1A.

Roa BB, Garcia CA, Wise CA, Anderson K, Greenberg F, Patel PI, Lupski JR.

Prog Clin Biol Res. 1993;384:187-205. Review. No abstract available.

PMID:
8115402
42.

Body composition studies in Prader-Willi syndrome: effects of growth hormone therapy.

Lee PD, Hwu K, Henson H, Brown BT, Bricker JT, LeBlanc AD, Fiorotto ML, Greenberg F, Klish WJ.

Basic Life Sci. 1993;60:201-5. No abstract available.

PMID:
8110110
43.

An association between fetal abdominal wall defects and elevated levels of human chorionic gonadotropin in mid-trimester.

Schmidt D, Rose E, Greenberg F.

Prenat Diagn. 1993 Jan;13(1):9-12. Erratum in: Prenat Diagn 1993 Apr;13(4):309.

PMID:
7680473
44.

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.

Kuwano A, Mutirangura A, Dittrich B, Buiting K, Horsthemke B, Saitoh S, Niikawa N, Ledbetter SA, Greenberg F, Chinault AC, et al.

Hum Mol Genet. 1992 Sep;1(6):417-25. Erratum in: Hum Mol Genet 1992 Dec;1(9):784.

PMID:
1363801
45.

Congenital deficiency of alpha-fetoprotein.

Greenberg F, Faucett A, Rose E, Bancalari L, Kardon NB, Mizejewski G, Haddow JE, Alpert E.

Am J Obstet Gynecol. 1992 Aug;167(2):509-11.

PMID:
1379776
46.

Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p.

Guzzetta V, Franco B, Trask BJ, Zhang H, Saucedo-Cardenas O, Montes de Oca-Luna R, Greenberg F, Chinault AC, Lupski JR, Patel PI.

Genomics. 1992 Jul;13(3):551-9.

PMID:
1639385
47.

Maternal serum alpha-fetoprotein, beta-human chorionic gonadotropin, and unconjugated estriol levels in midtrimester trisomy 18 pregnancies.

Greenberg F, Schmidt D, Darnule AT, Weyland BR, Rose E, Alpert E.

Am J Obstet Gynecol. 1992 May;166(5):1388-92.

PMID:
1375811
48.

Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia using the polymerase chain reaction.

Owerbach D, Draznin MB, Carpenter RJ, Greenberg F.

Hum Genet. 1992 Apr;89(1):109-10.

PMID:
1349559
49.

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A.

Lupski JR, Wise CA, Kuwano A, Pentao L, Parke JT, Glaze DG, Ledbetter DH, Greenberg F, Patel PI.

Nat Genet. 1992 Apr;1(1):29-33.

PMID:
1301995
50.

Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.

McGinniss MJ, Kazazian HH Jr, Stetten G, Petersen MB, Boman H, Engel E, Greenberg F, Hertz JM, Johnson A, Laca Z, et al.

Am J Hum Genet. 1992 Jan;50(1):15-28.

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