(Q36216336)

12 August 2017

1 reference

title

Terminological, Diagnostic, Nosological, and Anatomical-Developmental Aspects of Developmental Defects in Man (English)

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

15 May 2022

1

Opitz JM

1 reference

12 August 2017

J. Herrmann

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A160752

15 May 2022

J. C. Pettersen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A160752

15 May 2022

E. T. Bersu

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A160752

15 May 2022

S. C. Colacino

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A160752

15 May 2022

language of work or name

1 reference

1 January 1979

1 reference

full work available at URL

12 August 2017

http://link.springer.com/content/pdf/10.1007/978-1-4615-8276-2_2

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Advances in human genetics

15 May 2022

published in

1 reference

12 August 2017

9

1 reference

12 August 2017

71-164

1 reference

Birth defects original article series

12 August 2017

4

6

3

BA Barash

1970

1 reference

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Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome ?A pathogenetic hypothesis

15 May 2022

10

122

1

ET Bersu

1976

1 reference

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Familial bilateral renal agenesis and hereditary renal adysplasia

15 May 2022

16

115

111

RM Buchta

1973

1 reference

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Locating genetic loci with aneuploids

15 May 2022

17

114

273

PS Carlson

1971

1 reference

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TRIPLOID-DIPLOID CHIMERISM IN A MALE TORTOISESHELL CAT

15 May 2022

20

3

1

EHY Chu

1964

1 reference

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Birth defects original article series

15 May 2022

21

7

125

MM Cohen Jr.

1971

1 reference

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Concepts of disease and diagnosis

15 May 2022

23

20

528

D Copeland

1977

1 reference

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Dosage effect of SOD-A gene in 21-trisomic cells

15 May 2022

24

31

197

N Crosti

1976

1 reference

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Birth defects original article series

15 May 2022

Mortality and skeletal malformations from amniocentesis and oligohydramnios in rats: Cleft palate, clubfoot, microstomia, and adactyly

27

volume

7

0 references

29

2

33

W DeMyer

1969

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Congenital postural deformities

15 May 2022

33

32

71

PM Dunn

1976

1 reference

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An unusual dysplasia-malformation-cancer syndrome in two patients

15 May 2022

34

1

279

MV Durkin-Stamm

1978

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

15 May 2022

A new trisomic syndrome

35

1

787

JH Edwards

1960

1 reference

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Teratogenesis of craniofacial malformations in animals. 3. Natural and experimental cephalic deformities in sheep.

15 May 2022

39

13

706

HE Evans

1966

1 reference

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Pattern regulation in epimorphic fields

15 May 2022

42

193

969

V French

1976

1 reference

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Vitamin D and the supravalvar aortic stenosis syndrome. The transplacental effects of vitamin D on the aorta of the rabbit

15 May 2022

43

34

77

EF Friedeman

1966

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Studies on deoxyribonucleic acid polymerase from normal and Down's syndrome skin fibroblasts in vitro.

15 May 2022

45

10

167

RE Giblak

1974

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

15 May 2022

47

1

1

W Gooddy

1961

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Trisomy in the fetal backcross progeny of male and female metacentric heterozygotes of the mouse. i

15 May 2022

48

13

511

A Gropp

1974

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Systematic approach to the study of trisomy in the mouse. II

15 May 2022

49

14

42

A Gropp

1975

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Visual pathways in albinos

15 May 2022

0 references

Biological regeneration and pattern formation

15

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Transdetermination in Cells

18 December 2022

56

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

The SC phocomelia and the Roberts syndrome: nosologic aspects

18 December 2022

62

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Studies of malformation syndromes of man XXXXI B: Nosologic studies in the Hanhart and the Möbius syndrome

18 December 2022

63

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Familial holoprosencephaly with endocrine dysgenesis.

18 December 2022

65

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Genetic heterogeneity of cebocephaly

18 December 2022

67

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Genetic control of development of the cellular slime mold, Dictyostelium discoideum

18 December 2022

69

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Intrauterine growth retardation

18 December 2022

71

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases

18 December 2022

76

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Further studies on the genetic heterogeneity of cebocephaly

18 December 2022

77

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Oxidative energy deficiency. II. Human achondroplasia

18 December 2022

84

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Autosomal trisomy in a chimpanzee: resemblance to Down's syndrome

18 December 2022

85

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Arhinencephaly and multiple developmental anomalies occurring in a human full-term foetus.

18 December 2022

94

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Studies of malformation syndromes XXVA. Phenotypic and genetic studies of the Brachmann-de Lange Syndrome

18 December 2022

95

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Studies of malformation syndromes of man XXXIX: a craniosynostosis-craniofacial dysostosis syndrome with mental retardation and other malformations: "craniofacial dyssynostosis".

18 December 2022

101

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Cornelia de Lange syndrome: evolution of the phenotype

18 December 2022

112

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Multiple congenital anomaly caused by an extra autosome

18 December 2022

113

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

A community of human malformation syndromes involving the müllerian ducts, distal extremities, urinary tract, and ears

18 December 2022

119

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

The community of human malformation syndromes that shares ectodermal dysplasia and deformities of the hands and feet

18 December 2022

120

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

5alpha-reductase activity of genital and nongenital skin fibroblasts from patients with 5alpha-reductase deficiency, androgen insensitivity, or unknown forms of male pseudohermaphroditism

18 December 2022

122

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

THE CELL CYCLE AND CHROMOSOME ANOMALIES

18 December 2022

124

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

The pathogenesis of the first and second branchial arch syndrome

18 December 2022

125

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

A screening test for patients suspected of having Turner syndrome

18 December 2022

126

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

A methodology for establishing a diagnostic index for syndromes of unknown etiology

18 December 2022

127

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Glossary of Genetics and Cytogenetics – Classical and Molecular

18 December 2022

130

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Control of developing fields

18 December 2022

132

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Replication rate and lifespan of cultured fibroblasts in Down's syndrome

18 December 2022

135

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

18 December 2022

[Syndromatology.]

136

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Studies on Down's syndrome in tissue culture. I. Growth rates and protein contents of fibroblast cultures

18 December 2022

137

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Amplified developmental instability in Down's syndrome

18 December 2022

139

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

[Overactivity of the indophenol oxidase (form dimeric) in the trisomy 21, secondary to triplicated gene (author's transl)].

18 December 2022

140

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

An approach to clinical dysmorphology

18 December 2022

141

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

The linkage of genes for the human interferon-induced antiviral protein and indophenol oxidase-B traits to chromosome G-21

18 December 2022

152

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

The Somatic Cell Genetics of Human Interferon: Assignment of Human Interferon Loci to Chromosomes 2 and 5

18 December 2022

153

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

A cytogenetic survey of 200 unclassifiable mentally retarded children with congenital anomalies and 200 normal controls

18 December 2022

156

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Spontaneous occurrence of chromosome abnormality in cats

18 December 2022

157

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis

18 December 2022

160

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Trisomy 19 in the laboratory mouse. I. Frequency in different crosses at specific developmental stages and relationship of trisomy to cleft palate.

18 December 2022

163

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Trisomy 19 in the laboratory mouse. II. Intra-uterine growth and histological studies of trisomics and their normal littermates

18 December 2022

164

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

Pathoarchitectonic studies of cerebral malformations. III. Arrhinencephalies (holotelencephalies).

18 December 2022

166

1 reference

https://api.crossref.org/works/10.1007/978-1-4615-8276-2_2

18 December 2022

Identifiers

0 references

1 reference