H. Punnett

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Induction of Leucocyte Growth in Cultures of Human Peripheral Blood

T. Punnett, H. Punnett, 1963, Nature.

Identification of Microdeletions Spanning the Diamond-Blackfan Anemia Locus on 19q13 and Evidence for Genetic Heterogeneity

Sarah E. Ball, Peter Gustavsson, Nancy F. Olivieri, 1998 .

Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal.

J. W. Foster, S. Mansour, O. Zuffardi, 1995, American journal of human genetics.

Lymphocytes in Congenital Absence of the Thymus

H. Punnett, H. Lischner, A. Digeorge, 1967, Nature.

Chromosome Rearrangement with No Apparent Gene Mutation in Familial Adenomatous Polyposis and Hepatocellular Neoplasia

A. Ganguly, U. Blecker, J. de Chadarévian, 2002, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Characterization of a Wilms tumor in a 9‐year‐old girl with trisomy 18

V. Huff, J. de Chadarévian, H. Punnett, 2003, American journal of medical genetics. Part A.

Citrullinemia, argininosuccinate synthetase deficiency. Repository identification No. GM-1044.

N. Kennaway, H. Punnett, A. Greene, 1977, Cytogenetics and cell genetics.

Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16.

L. Ala‐Kokko, A. Christiano, H. Kuivaniemi, 1996, American journal of human genetics.

FOXO1–FGFR1 fusion and amplification in a solid variant of alveolar rhabdomyosarcoma

P. Papenhausen, H. Punnett, M. Guzmán, 2011, Modern Pathology.

Analysis of fetal intestinal enzymes in amniotic fluid for the prenatal diagnosis of cystic fibrosis.

E. Pergament, F. Muller, D. Cook, 1987, American journal of human genetics.

IDENTIFICATION OF MICRODELETIONS SPANNING THE DIAMOND-BLACKFAN ANEMIA (DBA) LOCUS ON 19Q13 AND EVIDENCE FOR GENETIC HETEROGENEITY

I. Dianzani, H. Cario, N. Olivieri, 1998, Pediatric Research.

Syndrome of ankylosis, facial anomalies, and pulmonary hypoplasia.

R. Ellison, M. Valdes-Dapena, H. Punnett, 1974, The Journal of pediatrics.

An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry.

B. Trask, G. van den Engh, R. Nussbaum, 1989, American journal of human genetics.

Possible graft-versus-host reaction after intrauterine transfusion for Rh erythroblastosis fetalis.

J. Arey, J. Naiman, H. Punnett, 1969, The New England journal of medicine.

Characterization of alternative amino acid substitutions at arginine 830 of the androgen receptor that cause complete androgen insensitivity in three families.

T. Brown, M. Kaufman, L. Pinsky, 1995, Human molecular genetics.

Consistency of Isochromosome 7q and Trisomy 8 in Hepatosplenic γδ T-cell Lymphoma: Detection by Fluorescence In Situ Hybridization of a Splenic Touch-Preparation from a Pediatric Patient

M. Koehler, M. Borowitz, C. Griffin, 1999, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

A new point mutation in the beta-hexosaminidase alpha subunit gene responsible for infantile Tay-Sachs disease in a non-Jewish Caucasian patient (a Kpn mutant).

K. Suzuki, H. Punnett, A. Tanaka, 1990, American journal of human genetics.

SERIAL CYTOGENETIC AND HEMATOLOGIC STUDIES ON A MONGOL WITH TRISOMY-21 AND ACUTE CONGENITAL LEUKEMIA.

H. Thiede, E. Charney, H. Punnett, 1964, Jornal de Pediatria.

Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia.

J. Morrissette, J. de Chadarévian, H. Punnett, 2006, Cancer genetics and cytogenetics.

Short communication Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia

H. Punnett, G. Halligan, F. Guerrero, 2006 .

A tribute to Thomas Roosevelt Punnett, Jr. (1926–2008)

Govindjee, L. Punnett, H. Punnett, 2011, Photosynthesis Research.

5p14 deletion associated with microcephaly and seizures

J. Overhauser, H. Punnett, R. Marinescu, 2000, Journal of medical genetics.

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

E. Zackai, B. Emanuel, R. Kelley, 1982, The Journal of pediatrics.

Maternal uniparental disomy of chromosome 21 in a normal child.

P. Rogan, H. Punnett, D. Sabol, 1999, American journal of medical genetics.

ETV6-NTRK3 gene fusion in metastasizing congenital fibrosarcoma.

P. Sorensen, B. Pawel, J. de Chadarévian, 2000, Medical and pediatric oncology.

PRENATAL DIAGNOSIS OF THE 22q11 DELETION SYNDROME

M. Khandelwal, H. Punnett, A. Davidson, 1997, Prenatal diagnosis.

Improvement of pancytopenia and thrombocytopenia with decreasing mosaicism for isochromosome Xp

J. Morrissette, J. de Chadarévian, H. Punnett, 2009, Pediatric blood & cancer.

AN IMPROVED SQUASH TECHNIQUE FOR HUMAN MALE MEIOTIC CHROMOSOMES: SOFTENING AND CONCENTRATION OF CELLS; MOUNTING IN HOYER'S MEDIUM.

H. Punnett, H. H. Gardner, 1964, Stain technology.

CYTOLOGICAL EVIDENCE OF HEXAPLOID CELLSIn Maize Endosperm

H. Punnett, 1953 .

OA1 mutations and deletions in X-linked ocular albinism.

K. Kidd, G. Quinn, S. Orlow, 1998, American journal of human genetics.

Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly

I. Hanson, T. Jordan, H. Punnett, 1994, Nature Genetics.

Clinical manifestations of familial 13;18 translocation.

W. Blattner, Shien Tsai, E. Giblett, 1980, Journal of medical genetics.

Comparative behavior of ring chromosomes.

H. Punnett, M. Kistenmacher, 1970, American journal of human genetics.

DELETION OF SHORT ARM OF CHROMOSOME 5.

H. Punnett, A. Digeorge, G. Carpenter, 1964, Lancet.

PREPARATION OF A CRUDE HUMAN LEUCOCYTE GROWTH FACTOR FROM PHASEOLIS VULGARIS

B. Kaufmann, T. Punnett, H. Punnett, 1962 .

A (7;18) translocation. 46,XY

H. Punnett, A. Greene, L. Coriell, 1979 .

A syndrome of ocular abnormalities, calcification of cartilage, and failure to thrive.

H. Punnett, J. Kirkpatrick, 1968, The Journal of pediatrics.

Globoid cells, glial nodules, and peculiar fibrillary changes in the cerebro‐hepato‐renal syndrome of zellweger

W. Grover, H. Punnett, D. Huff, 1977, Annals of neurology.

A report of three patients with an interstitial deletion of chromosome 15q24

A. Cherry, O. Abdul-Rahman, G. Vance, 2005, American journal of medical genetics. Part A.

Reproductive risks for carriers of complex chromosome rearrangements: analysis of 25 families.

E. Zackai, B. Emanuel, J. Gorski, 1988, American journal of medical genetics.

Diaphragmatic hernia in tetrasomy 12p mosaicism.

E. Zackai, E. Ruchelli, J. Bergoffen, 1993, The Journal of pediatrics.

Standardized karyotype of deer mice, Peromyscus (Rodentia)

T. Shows, F. Arrighi, G. Donnell, 1977 .

Old Syndromes and New Cytogenetics

H. Punnett, E. Zakai, Elaine H. Zakai, 1990, Developmental medicine and child neurology.

Confirmation of prenatally ascertained trisomy 20 mosaicism

H. Punnett, M. Kistenmacher, 1990, Prenatal diagnosis.

Co‐occurrence of non‐mosaic trisomy 22 and inherited balanced t(4;6)(q33;q23.3) in a liveborn female: Case report and review of the literature

H. Punnett, J. Pascasio, C. Anderson, 2014, American journal of medical genetics. Part A.

Quinacrine fluorescence and Giemsa banding in trisomy 22

G. Kohn, H. Punnett, M. Kistenmacher, 2004, Theoretical and Applied Genetics.

The Russell-Silver Syndrome? Or Trisomy 18?

H. Punnett, M. Kistenmacher, A. Pileggi, 1973, Pediatrics.

An (X;1) translocation, balanced, 46 chromosomes

H. Punnett, A. Greene, L. Coriell, 1974 .

Definition of heterozygosity.

H. Punnett, 1982, The Journal of pediatrics.

Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype.

B. Emanuel, M. Budarf, D. Driscoll, 1998, American journal of human genetics.

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

P. Bray-Ward, D. Ward, J. Wienberg, 1996, Human molecular genetics.

Hunter syndrome in girl.

H. Punnett, 1973, The New England journal of medicine.

Limitations of metachromasia as a diagnostic aid in pediatrics.

K. Taysi, H. Punnett, M. Kistenmacher, 1969, The New England journal of medicine.

Hyperdiploidy and trisomy 12 in the cystic partially differentiated nephroblastoma.

D. Billmire, J. de Chadarévian, H. Punnett, 1996, Human pathology.

Focal dermal hypoplasia syndrome in a male

H. Punnett, A. Digeorge, M. Kistenmacher, 1975 .

Letter: Testicular feminisation and inguinal hernia.

H. Punnett, M. Kistenmacher, M. Toro-Sola, 1973, Lancet.

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fcγ receptor gene region

M. King, T. Bird, R. Lovelace, 1991, Human Genetics.

Cytogenetic analysis of a choroid plexus papilloma

J. de Chadarévian, P. Kanev, H. Punnett, 1994, Genes, chromosomes & cancer.

Consistent aneuploidies in choroid plexus papillomas

H. Punnett, E. Tomczak, J. P. Chadarévian, 1999, Genes, Chromosomes and Cancer.

Translocation (16;18)(p13;q21.3) in follicular lymphoma.

P. Crilley, M. Mahmoodi, H. Punnett, 2004, Cancer genetics and cytogenetics.

A ring 9 chromosome. Repository identification no. GM-166.

H. Punnett, A. Greene, L. Coriell, 1975, Cytogenetics and cell genetics.

Abnormalities of the sex chromosome complement in man

H. Punnett, 1965 .

Fine structure of skeletal dysplasia as seen in pseudoachondroplastic spondyloepiphyseal dysplasia and asphyxiating thoracic dystrophy.

H. Punnett, M. Kistenmacher, R. D. Campo, 1974, Birth defects original article series.

IMPORTANCE OF PATHOLOGICAL EXAMINATION OF PRODUCTS OF CONCEPTION WHICH ARE DELIVERED AFTER PRENATAL SCREENING PROCEDURES

H. Punnett, DaleS. Huff, 1982, The Lancet.

PHYTOHÆMAGGLUTININ AND THYMIC LYMPHOCYTES

H. Punnett, H. Lischner, 1966 .

Translocation 10;17 in clear cell sarcoma of the kidney. A first report.

H. Punnett, G. Halligan, N. Karmazin, 1989, Cancer genetics and cytogenetics.

Carrier detection in cystic fibrosis.

H. Punnett, A. Qureshi, 1985, The Journal of pediatrics.

R. Dalgleish, A. Paepe, B. Steinmann, 1994, Human Genetics.

An improved method for phenotyping of alpha 1-antitrypsin variants using separator isoelectric focusing on thin-layer agarose gel.

H. Punnett, A. Qureshi, 1982, Analytical biochemistry.

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fcγ receptor gene region

M. King, T. Bird, R. Lovelace, 2004, Human Genetics.

MEDICAL GENETICS 1962.

V. McKusick, E. Murphy, W. M. Ginn, 1963, Journal of chronic diseases.

Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and Genomics

S. Schwartz, F. Bieber, R. Stevenson, 2016, Genetics in Medicine.

Deletion of the Long Arm of Chromosome 16 and an Unexpected Duffy Blood Group Phenotype reveal a Possible Autosomal Linkage

M. N. Crawford, H. Punnett, G. Carpenter, 1967, Nature.

Genetic Linkage ofFamilial Granulomatous Inflammatory Arthritis, SkinRash, andUveitis toChromosome 16

A. Christiano, H. Kuivaniemi, G. Tromp, 1996 .