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Heritable fragile sites and lymphocyte culture medium containing BrdU. Am J Hum Genet (1980) 1.73

The importance of being a fragile site. Am J Hum Genet (1979) 1.57

Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation. Hum Genet (1980) 1.46

Postexposure prophylaxis after nonoccupational HIV exposure: clinical, ethical, and policy considerations. JAMA (1998) 2.58

Parthenogenic origin of benign ovarian teratomas. N Engl J Med (1975) 2.53

Congenital contractural arachnodactyly. A heritable disorder of connective tissue. J Bone Joint Surg Am (1971) 2.24

Common region on chromosome 14 in T-cell leukemia and lymphoma. Science (1984) 1.98

Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man. Science (1970) 1.87

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Somatic rearrangement of chromosome 14 in human lymphocytes. Proc Natl Acad Sci U S A (1975) 1.61

Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis. Hum Genet (1989) 1.60

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XXY cells in a predominantly XX human male: evidence for cell selection. Pediatrics (1966) 1.51

Non-random occurrence of 7-14 translocations in human lymphocyte cultures. Nature (1975) 1.41

Estimating distances from the centromere by means of benign ovarian teratomas in man. Ann Hum Genet (1976) 1.40

"New" syndrome of congenital contractural arachnodactyly originally described by Marfan in 1896. Pediatrics (1972) 1.40

Seizure disorders in the fragile X chromosome syndrome. Am J Med Genet (1991) 1.39

Mutations of the Kirsten-ras proto-oncogene in human preleukaemia. Nature (1987) 1.35

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Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation. Clin Genet (1987) 1.33

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Partial trisomy 15. Lancet (1972) 1.29

Long-term growth of malignant thymocytes in vitro. Blood (1989) 1.28

Cancer chromosome breakpoints and common fragile sites induced by aphidicolin. Cancer Genet Cytogenet (1984) 1.22

Common mechanism of chromosome inversion in B- and T-cell tumors: relevance to lymphoid development. Science (1986) 1.21

Histiocytic lymphoma cell lines: immunologic and cytogenetic studies. Cancer Genet Cytogenet (1985) 1.21

A surgical approach to the treatment of fetal hydrocephalus. N Engl J Med (1982) 1.18

Nonrandomness of translocations in man: preferential entry of chromosomes into 13-15-21 translocations. Science (1968) 1.17

Chromosome 3 duplication q/deletion p syndrome. Pediatrics (1978) 1.17

Ataxia-telangiectasia--clonal growth of translocation lymphocytes. N Engl J Med (1973) 1.17

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Heritable dysmorphic syndrome with normal intelligence. J Pediatr (1967) 1.13

The Interregional Cytogenetic Register System (ICRS). Birth Defects Orig Artic Ser (1978) 1.13

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What we don't know about genetic counseling. N Engl J Med (1972) 1.09

Clinical and biologic characterization of T-cell neoplasias with rearrangements of chromosome 7 band q34. Blood (1988) 1.09

Lysergic-acid-diethylamide and cannabis as possible teratogens in man. Lancet (1968) 1.08

Little heads: inheritance and early detection. J Pediatr (1979) 1.07

Three additional cases of the congenital hypothalamic "hamartoblastoma" (Pallister-Hall) syndrome. Am J Med Genet (1989) 1.06

Ring 22 chromosomes in dermatofibrosarcoma protuberans are low-level amplifiers of chromosome 17 and 22 sequences. Cancer Res (1995) 1.06

Fragile sites and cancer breakpoints. Cancer Genet Cytogenet (1984) 1.05

Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements. Am J Hum Genet (1971) 1.04

A rearranged transforming gene, tre, is made up of human sequences derived from chromosome regions 5q, 17q and 18q. Oncogene (1988) 1.04

Tort liability in genetic diagnosis and genetic counseling. Am J Hum Genet (1982) 1.04

Double aneuploidy: the frequency of XXY in males with Down's syndrome. Am J Hum Genet (1969) 1.04

Congenital cutis laxa with retardation of growth and motor development: a recessive disorder of connective tissue with male lethality. Clin Genet (1986) 1.04

Neurofibromatosis and malignancy. J Pediatr (1979) 1.02

Annotation: genetic effects of aneuploidy. Am J Hum Genet (1973) 1.00

Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II. Ann Genet (1972) 1.00

Familial predisposition to thyroid disease in Down's syndrome: controlled immunoclinical studies. Am J Hum Genet (1971) 0.99

Impaired in vitro response of circulating lymphocytes to phytohemagglutinin in Down's syndrome: dose- and time-response curves and relation to cellular immunity. Int Arch Allergy Appl Immunol (1970) 0.99

IgA and partial deletions of chromosome 18. Lancet (1969) 0.98

Regional chromosome localization of human papillomavirus integration sites near fragile sites, oncogenes, and cancer chromosome breakpoints. Cancer Genet Cytogenet (1988) 0.98

A confirmatory factor analysis of the WISC-III in a clinical sample with cross-validation in the standardization sample. Child Neuropsychol (2001) 0.96

Human benign ovarian teratomas: chromosomal and electrophoretic enzyme studies. Birth Defects Orig Artic Ser (1978) 0.95

Nomenclature: the Philadelphia chromosome or Ph without superscript. Cancer Genet Cytogenet (1985) 0.95

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Chromosome subband 17p11.2 deletion: a minute deletion syndrome. J Med Genet (1988) 0.95

Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome. J Med Genet (1970) 0.94

Acute myeloblastic leukemia (AML) with t(6;9) (p23;q34): a specific subgroup of AML? Cancer Genet Cytogenet (1983) 0.94

Ovarian teratomas: cytologic data. Cytogenet Cell Genet (1976) 0.94

Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+). Cytogenetics (1971) 0.94

Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia. Cancer Genet Cytogenet (1981) 0.92

Telomeric fusion in pre-T-cell acute lymphoblastic leukemia. Hum Genet (1986) 0.92

Racial differences in the frequency of Q and C chromosomal heteromorphisms. Nature (1977) 0.92

Amniocyte clones for prenatal cytogenetics. Am J Med Genet (1981) 0.92

Mosaicism in Turner's syndrome reflects the lethality of XO. Lancet (1969) 0.90

Fragile sites limited to lymphocytes: molecular recombination and malignancy. Cancer Genet Cytogenet (1987) 0.89

Chromosomes in kidney, ureter, and bladder cancer. Cancer Genet Cytogenet (1986) 0.89

The half chromatid mutation model and bidirectional mutation in incontinentia pigmenti. Clin Genet (1983) 0.89

Ovarian teratomas and genetics of germ-cell formation. Lancet (1976) 0.89

Supernumerary ring chromosomes containing chromosome 17 sequences. A specific feature of dermatofibrosarcoma protuberans? Cancer Genet Cytogenet (1994) 0.88

Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis. Clin Genet (1984) 0.88

Translocations in T-cell leukemia in lymphoma. N Engl J Med (1985) 0.88

Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh. Birth Defects Orig Artic Ser (1975) 0.88

Philadelphia chromosome-positive acute lymphoblastic leukemia cell lines without classical breakpoint cluster region rearrangement. Cancer Res (1988) 0.88

Chromosome 14 translocation in African and North American Burkitt's lymphoma;. Int J Cancer (1977) 0.87

The fragile X chromosome: current methods. Am J Med Genet (1982) 0.87

Transformation of blood lymphocytes in ataxia telangiectasia. Dose and time response to phytohemagglutinin. Int Arch Allergy Appl Immunol (1970) 0.87

Detection of fragile sites on human chromosomes. Clin Genet (1985) 0.87

Who will survive with trisomy 13 or 18? A call for cases 10 years old or above. Am J Med Genet (1981) 0.87

Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes. Cancer Genet Cytogenet (1988) 0.87

Giemsa banding pattern of a heritable 1q+ variant chromosome: a possible partial duplication. J Med Genet (1972) 0.87

Construction of long-range restriction maps in human DNA using pulsed field gel electrophoresis. Gene Anal Tech (1989) 0.86

Incontinentia pigmenti in Arizona Indians including transmission from mother to son inconsistent with the half chromatid mutation model. Clin Genet (1982) 0.85

Origin of extragonadal teratomas and endodermal sinus tumours. Nature (1975) 0.85

Hereditary intestinal neurofibromatosis. I. A distinctive genetic disease. Neurofibromatosis (1988) 0.85

The Philadelphia chromosome: a model of cancer and molecular cytogenetics. Cancer Genet Cytogenet (1986) 0.84

The fragile site hypothesis of cancer. Cancer Genet Cytogenet (1988) 0.83

Fetal loss after chorionic villus sampling (CVS) in small and large centres. Prenat Diagn (1985) 0.83

Detection of the fragile X chromosome and other fragile sites. Clin Genet (1984) 0.83

Chromosome 5q35 breakpoint in malignant histiocytosis. N Engl J Med (1986) 0.83

Sacrococcygeal teratoma: prenatal diagnosis with elevated alphafetoprotein and acetylcholinesterase in amniotic fluid. Prenat Diagn (1982) 0.83

Trisomy 4: an entity within acute nonlymphocytic leukemia. Cancer Genet Cytogenet (1987) 0.83

Aneuploidy in recurrent spontaneous aborters: the tendency to parental nondisjunction. Clin Genet (1984) 0.82