(Q39945272)

15 September 2017

title

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

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

19 May 2022

author name string

Pinsky L

1

1 reference

15 September 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=168661

19 May 2022

publication date

1 June 1975

1 reference

full work available at URL

15 September 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Ftera.1420110302

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

https://onlinelibrary.wiley.com/doi/full/10.1002/tera.1420110302

19 May 2022

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Birth Defects Research Part A: Clinical and Molecular Teratology

19 May 2022

published in

1 reference

15 September 2017

11

3

227–42

June 1975

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=168661

19 May 2022

volume

11

1 reference

15 September 2017

issue

3

1 reference

15 September 2017

page(s)

227-242

1 reference

A new dental, ocular and cutaneous syndrome

15 September 2017

cites work

1

12

285

Ackerman

1973

1 reference

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Knuckle pads, leukonychia and deafness. A dominantly inherited syndrome

19 May 2022

4

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Bart

1967

1 reference

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Hypertelorism, microtia, and facial clefting. A newly described inherited syndrome

19 May 2022

7

118

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Bixler

1969

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

The ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome. Report of 2 cases and review of the literature.

19 May 2022

8

3

43

Bixler

1972

1 reference

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Phenotypic variation in the popliteal pterygium syndrome

19 May 2022

9

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220

Bixler

1973

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases

19 May 2022

10

24

151

Blank

1960

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

The syndrome of ectrodactyly, ectodermal dysplasia and cleft lip and palate: report of a family demonstrating a dominant inheritance pattern

19 May 2022

13

3

295

Brill

1972

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

19 May 2022

Incontinentia pigmenti

15

102

157

Carney

1970

1 reference

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Letter: The demise of the Marshall syndrome

19 May 2022

18

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Cohen

1974

1 reference

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Nature and etiology of the Poland anomaly

19 May 2022

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David

1972

1 reference

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Unilateral limb and skin deformities with congenital heart disease in two siblings: A lethal syndrome

19 May 2022

Congenital deafness associated with onychodystrophy.

22

0 references

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74

507

Feinmesser

1961

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

19 May 2022

Ectodermal Dysplasias

25

21

309

Freire-Maia

1971

1 reference

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Ectrodactyly‐ectodermal dysplasia‐clefting (EEC) syndrome

19 May 2022

26

3

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Fried

1972

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

The “tooth and nail” type of autosomal dominant ectodermal dysplasia

19 May 2022

29

37

576

Giansanti

1974

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Single atrium and the Ellis-van Creveld syndrome

19 May 2022

31

62

558

Giknis

1963

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Frontometaphyseal dysplasia. A new syndrome

19 May 2022

34

118

595

Gorlin

1969

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Heritable dysmorphic syndrome with normal intelligence

19 May 2022

41

70

927

Hecht

1967

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

The lacrimo-auriculo-dento-digital syndrome

19 May 2022

45

83

438

Hollister

1973

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

A syndrome of congenital aplasia of the alae nasi, deafness, hypothyroidism, dwarfism, absent permanent teeth, and malabsorption

19 May 2022

46

79

982

Johanson

1971

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Dental abnormalities in the tricho-dento-osseous syndrome

19 May 2022

47

36

693

Jorgenson

1973

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

A new familial syndrome of oral, cranial, and digital anomalies

19 May 2022

48

74

755

Juberg

1969

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Ectrodactyly, ectodermal dysplasia, and clefting syndrome

19 May 2022

49

76

992

Kaiser-Kupfer

1973

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Anonychia with ectrodactyly: clinical and linkage data

19 May 2022

53

22

69

Lees

1958

0 references

Lobster-claw deformities of the hands and feet

55

23

269

Maisels

1970

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Congenital Deafness, Spiny Hyperkeratosis, and Universal Alopecia

19 May 2022

61

93

68

Myers

1971

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

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

19 May 2022

63

9

65

Pinsky

1974

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

19 May 2022

65

43

319

Porter

1968

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

The lobster claw defect with ectodermal defects, cleft lip-palate, tear duct anomaly and renal anomalies.

19 May 2022

66

4

369

Preus

1973

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Anhidrotic ectodermal dysplasia: autosomal dominant inheritance with palate and lip anomalies

19 May 2022

68

5

269

Rapp

1968

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Hereditary syndromes with auditory and dermatological manifestations

19 May 2022

69

95

456

Reed

1967

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Genetic and clinical heterogeneity in the oral-facial-digital syndromes

19 May 2022

71

71

94

Rimoin

1967

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Pili torti and sensory neural hearing loss.

19 May 2022

72

70

621

Robinson

1967

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome. Its association with conductive hearing loss

19 May 2022

75

82

107

Robinson

1973

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

19 May 2022

76

14

190

Rosselli

1961

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Hereditary hearing loss with saddle-nose and myopia.

19 May 2022

78

92

95

Ruppert

1970

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Familial hand abnormality and sensori-neural deafness: A new syndrome

19 May 2022

84

78

102

Stewart

0 references

Congenital absence of the breasts

86

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies

20 December 2022

88

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

THE SYNDROMES OF CLEFT LIP, CLEFT PALATE AND LOBSTER-CLAW DEFORMITIES OF HANDS AND FEET

20 December 2022

90

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

Ectodermal dysplasia and multiple defects (Rapp-Hodgkins type).

20 December 2022

92

1 reference

https://api.crossref.org/works/10.1002/TERA.1420110302

20 December 2022

Identifiers

1 reference

15 September 2017

1 reference