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Items: 1 to 50 of 78

1.

Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.

Wallerstein R, Yu MT, Neu RL, Benn P, Lee Bowen C, Crandall B, Disteche C, Donahue R, Harrison B, Hershey D, Higgins RR, Jenkins LS, Jackson-Cook C, Keitges E, Khodr G, Lin CC, Luthardt FW, Meisner L, Mengden G, Patil SR, Rodriguez M, Sciorra LJ, Shaffer LG, Stetten G, Van Dyke DL, Wang H.

Prenat Diagn. 2000 Feb;20(2):103-22.

PMID:
10694683
2.

Prenatal diagnosis of a familial interchromosomal insertion of Y chromosome heterochromatin.

Ashton-Prolla P, Gershin IF, Babu A, Neu RL, Zinberg RE, Willner JP, Desnick RJ, Cotter PD.

Am J Med Genet. 1997 Dec 31;73(4):470-3.

PMID:
9415476
3.

Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.

Hsu LY, Yu MT, Neu RL, Van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, Kalousek DK, Pantzar TJ, Wyatt P.

Prenat Diagn. 1997 Mar;17(3):201-42.

PMID:
9110367
4.

Trisomy 17 detected in amniotic fluid cells but not in newborn infant.

Butler MG, Neu RL, Mitchell K.

Am J Med Genet. 1996 Oct 28;65(3):247-8. No abstract available.

5.

Prenatal cytogenetic results from cases referred for 44 different types of abnormal ultrasound findings.

Hanna JS, Neu RL, Lockwood DH.

Prenat Diagn. 1996 Feb;16(2):109-15.

PMID:
8650120
6.

Difficulties in prenatal detection of mosaic trisomy 8.

Hanna JS, Neu RL, Barton JR.

Prenat Diagn. 1995 Dec;15(12):1196-7. No abstract available.

PMID:
8750306
7.
8.

Cleft palate and complex chromosome rearrangements.

Kousseff BG, Papenhausen P, Neu RL, Essig YP, Saraceno CA.

Clin Genet. 1992 Sep;42(3):135-42. Review.

PMID:
1327590
9.

A liveborn infant with tetraploidy.

Lafer CZ, Neu RL.

Am J Med Genet. 1988 Oct;31(2):375-8. Review.

PMID:
3068989
10.

Trisomy 3p23----pter and monosomy 11q23----qter in an infant with two translocation carrier parents.

Neu RL, Kousseff BG, Hardy DE, Essig YP, Miller KL, Jervis GA, Tedesco TA.

J Med Genet. 1988 Sep;25(9):631-3.

11.

Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomalies.

Neu RL, Kousseff BG, Madan S, Essig YP, Miller K, Tedesco TA.

Clin Genet. 1988 Feb;33(2):73-7.

PMID:
3359669
12.

Prenatal diagnosis of inv(X)(q12q28) in a male fetus.

Neu RL, Brar HS, Koos BJ.

J Med Genet. 1988 Jan;25(1):52-3.

13.

Ultrasound identification of apparently normal male genitalia in a 46,X,+mar fetus.

Neu RL, O'Brien WF, Kousseff BG, Tedesco TA, Farmelo MJ, Essig YP, Miller KL, Nichols PM.

J Med Genet. 1987 Dec;24(12):782-3.

14.

A 1q42 deletion in a Vietnamese infant.

Neu RL, Avila DA, Reddington JM.

Ann Genet. 1982;25(3):154-5. No abstract available.

PMID:
6982664
15.
16.

Brief clinical report: an infant with duplication of 17q21 lead to 17qter.

Gallien JU, Neu RL, Wynn RJ, Steinberg-Warren N, Bannerman RM.

Am J Med Genet. 1981;8(1):111-5.

PMID:
7246600
17.

An infant with trisomy 6q21 leads to 6qter.

Neu RL, Gallien JU, Steinberg-Warren N, Wynn RJ, Bannerman RM.

Ann Genet. 1981;24(3):167-9.

PMID:
6974528
19.

Minor hazard of amniocentesis.

Neu RL, Lanman JT Jr, Wingate M, Bannerman RM.

Br Med J. 1979 Mar 31;1(6167):893-4. No abstract available.

20.

Chromosome analysis in cases with repeated spontaneous abortions.

Neu RL, Entes K, Bannerman RM.

Obstet Gynecol. 1979 Mar;53(3):373-5.

PMID:
424112
21.

An infant with trisomy 9pter yields 9q22 resulting from 3:1 segregation in a 46,XX t(1;9) (p36;q22) mother.

Neu RL, Dennis NR, Lanman JT Jr, Bannerman RM.

Ann Genet. 1979;22(3):151-4.

PMID:
316670
22.

Duplication 2q33 leads to 2q37 due to paternal ins (12;2) translocation.

Dennis NR, Neu RL, Bannerman RM.

Am J Med Genet. 1978;1(3):271-7.

PMID:
677166
23.

The X isochromosome-X syndrome [46,X,i(Xq)]. Report of three cases with review of the phenotype.

Santana JA, Gardner LI, Neu RL.

Clin Pediatr (Phila). 1977 Nov;16(11):1021-6.

PMID:
913006
24.

A t(5p-;21q+) translocation in a family with Down syndrome.

Neu RL, DeGeorge FV, Gardner LI.

Clin Genet. 1977 Aug;12(2):111-3.

PMID:
142593
25.

A case of cyclopia with D trisomy.

Neu RL, Grant JF, Gardner LI.

Am J Obstet Gynecol. 1977 Jan 15;127(2):212-3. No abstract available.

PMID:
401559
26.

Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.

Neu RL, Ortega CC, Barg GA, Pinto W Jr, Gardner LI, Howell WM, Denton TE.

J Med Genet. 1976 Dec;13(6):520-2.

27.

46,XY/46,XY,21q- mosaicism in an infant with neutropenia and properdin deficiency.

Neu RL, Stockman JA, Spitzer RE, Tomar RH.

J Med Genet. 1976 Aug;13(4):332-4.

28.

Care of the pre-school handicapped.

Weinberg AD, Neu RL.

Lancet. 1975 Dec 27;2(7948):1303-4. No abstract available.

PMID:
54820
29.

Segregation of a t(14q22q) chromosome in a large kindred.

Neu RL, Valentine FA, Gardner LI.

Clin Genet. 1975 Jul;8(1):30-6.

PMID:
1149319
30.

4p- phenotype in an infant with t(4p-;19p or q+)mat translocation.

Neu RL, Shott RJ, Gardner LI.

Am J Dis Child. 1975 Mar;129(3):363-5.

PMID:
1121967
31.

X-chromosome banding in Noonan syndrome.

Barlow MJ Jr, Neu RL, Gardner LI.

Am J Dis Child. 1973 Nov;126(5):656-7. No abstract available.

PMID:
4126797
32.

Communications and commentaries: A 46,XYq- male with aspermia.

Neu RL, Barlow MJ Jr, Gardner LI.

Fertil Steril. 1973 Oct;24(10):811-3. No abstract available.

PMID:
4742003
33.

A partial trisomy of chromosome 1 in a family with a t(1q-;4q+) translocation.

Neu RL, Gardner LI.

Clin Genet. 1973 Jun;4(6):474-9. No abstract available.

PMID:
4787838
34.

Three generations and six family members with a t(13q15q) chromosome.

Neu RL, Gardner LI, Williams ML, Barlow MJ.

J Med Genet. 1973 Mar;10(1):94-6. No abstract available.

35.

A case of 46,XY,5(3q-;14q+)Mat.

Neu RL, Barlow MJ Jr, Gardner LI.

Clin Genet. 1973;4(2):158-61. No abstract available.

PMID:
4730945
36.

Normal Y chromosome fluorescent pattern in testicular feminization.

Neu RL, Gardner LI.

Am J Obstet Gynecol. 1972 Dec 1;114(7):932-3. No abstract available.

PMID:
4566570
37.

Banding patterns of the Y chromosome.

Neu RL, Gardner LI.

Lancet. 1972 May 6;1(7758):1020. No abstract available.

PMID:
4112345
38.

Lack of damage to human chromosomes and dimethyl mercury.

Kasputis D, Neu RL, Gardner LI, Skerfving S.

Arch Environ Health. 1972 May;24(5):378. No abstract available.

PMID:
5021123
39.

Evidence linking an extra Y chromosome to sociopathic behavior.

Gardner LI, Neu RL.

Arch Gen Psychiatry. 1972 Mar;26(3):220-2. No abstract available.

PMID:
5059633
40.

Clinical aspects of abnormalities of the X and Y chromosomes.

Neu RL, Gardner LI.

Clin Obstet Gynecol. 1972 Mar;15(1):141-56. Review. No abstract available.

PMID:
4556548
41.

Three families with abnormal, inherited chromosomes: 2q+mat, t(Cp+; 13q-)mat and t(3?-;5q+)pat.

Neu RL, Gardner LI.

Ann Genet. 1972 Mar;15(1):19-23. No abstract available.

PMID:
4402505
42.

Giemsa staining of heterochromatic areas of human chromosomes for identification.

Frey JP, Neu RL, Powers HO, Gardner LI.

Can J Genet Cytol. 1972 Mar;14(1):195-7. No abstract available.

PMID:
4113353
43.

A case of 47,XX,(21q-)+ with some stigmata of Down's syndrome and an IQ of 77.

Neu RL, Voorhess ML, Gardner LI.

J Med Genet. 1971 Dec;8(4):528-9. No abstract available.

44.

A case of 48,XXY,21+ in an infant with Down's syndrome.

Neu RL, Scheuer AQ, Gardner LI.

J Med Genet. 1971 Dec;8(4):533-5. No abstract available.

45.

Syndrome of multiple osseous defects with pretibial dimples.

Gardner LI, Assemany SR, Neu RL.

Lancet. 1971 Jul 10;2(7715):98. No abstract available.

PMID:
4104009
46.

A single nasal orifice and severe intrauterine growth retardation in a case of 46, XX, 18 r.

Neu RL, Watanabe N, Gardner LI, Galvis AG.

Ann Genet. 1971 Jun;14(2):139-42. No abstract available.

PMID:
5314801
47.

47,XX,13+ with Snodgrass phenotype II. Are different chromosomes associated with two clinical varieties of D-trisomy?

Neu RL, Assemany SR, Gardner LI.

J Med Genet. 1971 Jun;8(2):179-80. No abstract available.

48.

A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings.

Neu RL, Kajii T, Gardner LI, Nagyfy SF.

Pediatrics. 1971 Mar;47(3):610-2. No abstract available.

PMID:
5547878
49.

XXXXY syndrome in a phenotypic male infant with associated cardiac abnormalities.

Assemany SR, Neu RL, Gardner LI.

Humangenetik. 1971;12(2):101-4. No abstract available.

PMID:
5568728
50.

Lack of chromosome aberrations in autism.

Wolraich M, Bzostek B, Neu RL, Gardner LI.

N Engl J Med. 1970 Nov 26;283(22):1231. No abstract available.

PMID:
5472949

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